| CTRI Number |
CTRI/2024/12/078043 [Registered on: 12/12/2024] Trial Registered Prospectively |
| Last Modified On: |
12/12/2024 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Medical Device |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
Comparison of patient satisfaction, Cost and treatment success in patients suffering from lower ureteric stones undergoing Extracorporeal Shockwave Lithotripsy or Ureteroscopic lithotripsy. |
|
Scientific Title of Study
|
Comparative study of patient reported Outcomes, Cost and Stone free rates of ESWL and URSL for lower ureteric stones:
A Randomized Control Trial
|
| Trial Acronym |
NIL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Jaydeep Jain |
| Designation |
Senior Resident |
| Affiliation |
All India Institute of Medical Sciences |
| Address |
Room no: 550, 5th floor, OPD building, AIIMS, jodhpur, Basni Industrial Area , 342005 AIIMS, jodhpur, Basni Industrial Area Jodhpur RAJASTHAN 342005 India |
| Phone |
9554038108 |
| Fax |
|
| Email |
jaydeepjain24@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Shiv Charan Navriya |
| Designation |
Associate Professor |
| Affiliation |
AIIMS Jodhpur |
| Address |
Room no: 550, 5th floor, OPD building, AIIMS, jodhpur, Basni Industrial Area, 342005
Jodhpur RAJASTHAN 342005 India |
| Phone |
9958365510 |
| Fax |
|
| Email |
buddingurologist@gmail.com |
|
Details of Contact Person Public Query
|
| Name |
Dr Jaydeep Jain |
| Designation |
Senior Resident |
| Affiliation |
All India Institute of Medical Sciences |
| Address |
Room no: 550, 5th floor, OPD building, AIIMS, jodhpur, Basni Industrial Area, 342005 AIIMS, jodhpur, Basni Industrial Area Jodhpur RAJASTHAN 342005 India |
| Phone |
9554038108 |
| Fax |
|
| Email |
jaydeepjain24@gmail.com |
|
|
Source of Monetary or Material Support
|
|
|
Primary Sponsor
|
| Name |
All India Institute of Medical Sciences |
| Address |
AIIMS Road, Basni Industrial Area, 342005 |
| Type of Sponsor |
Government medical college |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Jaydeep Jain |
AIIMS Jodhpur |
Room no: 550, 5th floor, OPD building
AIIMS, jodhpur, BASNI INDUSTRIAL AREA Jodhpur RAJASTHAN |
9554038108
jaydeepjain24@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| Institutional Ethics Committee |
Approved |
|
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Regulatory Clearance Status from DCGI
|
|
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Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: N201||Calculus of ureter, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Comparator Agent |
ESWL |
Extracorporeal shockwave lithotripsy |
| Intervention |
URSL |
Ureteroscopic Lithotripsy |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
99.00 Year(s) |
| Gender |
Both |
| Details |
1. Presence of lower ureteric stone confirmed by CT KUB
2. Patients with a ureteric stone requiring active intervention
3. Adults aged ≥ 18 years
4. Suitable for either ESWL or ureteroscopic treatment
|
|
| ExclusionCriteria |
| Details |
1. Patients who are unable to provide consent
2. Radiolucent stones
3. Active urinary tract infections
4. Pregnancy
5. Uncontrolled hypertension
6. Uncontrolled bleeding tendencies
7. Severe skeletal malformations
8. Vascular malformations within the vicinity of the stone (such as iliac artery aneurysms)
9. Unable to assume the appropriate position (prone or supine) for ESWL
10. Solitary kidneys
11. Transplanted kidneys
|
|
|
Method of Generating Random Sequence
|
Permuted block randomization, fixed |
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Method of Concealment
|
Not Applicable |
|
Blinding/Masking
|
Not Applicable |
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Primary Outcome
|
| Outcome |
TimePoints |
1. Stone free rates at 1 week, 8 weeks and 3 months post intervention in both groups
2. Acceptability and patient satisfaction of received procedure at eight weeks post enrollment.
|
1 week
8 weeks and
3 months post intervention in both groups
|
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
SECONDARY OBJECTIVES
1. Additional interventions required up to three months post primary intervention.
2. Complications observed in both groups up to three months post intervention.
3. Acceptability and patient satisfaction of received procedure at eight weeks post enrollment.
4. Loss of working days for the management of the lower ureteric calculus.
5. Pain intensity and analgesic requirement at pre intervention, during intervention, at one week post intervention and at eight weeks post enrollment.
6. Functional generic health and wellbeing (SF-12), at eight weeks and at three months post enrollment.
|
one week
2 months
3 months |
|
|
Target Sample Size
|
Total Sample Size="160" Sample Size from India="160"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
N/A |
|
Date of First Enrollment (India)
|
31/12/2024 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="2" Months="6" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Urinary stone disease is very common with an
estimated prevalence among the general population of 2–3%. Ureteric stones are
associated with severe pain as they pass through the urinary tract and have
significant impact on patients’ quality of life due to the detrimental effect
on their ability to work and need for hospitalisation. Most ureteric stones can
be expected to pass spontaneously with supportive care. However, between
one-fifth and one-third of cases require an intervention. (1)
The two standard active intervention options
are extracorporeal shockwave lithotripsy (ESWL) and ureteroscopic stone
retrieval. ESWL and ureteroscopy are effective in terms of stone clearance;
however, they differ in terms of invasiveness, anaesthetic requirement,
treatment setting, complications, patient-reported outcomes (e.g. pain after
intervention, time off work) and cost.(2) There is uncertainty around which is
the most clinically effective in terms of stone clearance and the true cost to
the patient and to society (in terms of impact on patient-reported health and
economic burden).
The aim of this trial is to determine whether
in adults with lower ureteric stones judged to require active treatment, ESWL
is not inferior, clinically, and is more cost-effective compared to
ureteroscopic treatment as the initial management option. (3)
REVIEW OF LITERATURE
A joint clinical guideline on the management of
ureteric stones by the European Association of Urology and the American
Urological Association [4] estimates
that 68% of stones ≤ 5 mm and 47% of stones 5–10 mm in size can be
expected to pass spontaneously and concluded that the majority of these stones
pass within four to six weeks of presentation. Stones in the distal ureter pass
more readily than stones located more proximally. Consequently, patients with
favourable features and with smaller sized stones in the lower ureter are
initially treated conservatively. Immediate active intervention occurs in those
patients with larger stones and unfavourable features who are deemed clinically
to be unsuitable for conservative treatment. Those who fail standard
conservative care or who subsequently develop complications also undergo later
active treatment. This can be ESWL, preliminary ureteric stenting with later
stone removal, ureteroscopy with stone retrieval or destruction (in situ
lithotripsy) or percutaneous nephrostomy insertion and later stone removal.
ESWL and ureteroscopic treatment require expensive equipment and urological
expertise. Both have been shown to be options that are safe and effective in a
number of studies. In clinical practice, urologists tend to favour ureteroscopy
over ESWL particularly for mid and lower ureteric stones due to perceived
higher rate of clinical stone clearance [5].
A Cochrane systematic review (2007) [5] comparing
the effectiveness of ESWL with ureteroscopic management of ureteric stones
identified seven randomised controlled trials (RCTs) involving a total of 732
participants. The results of this review suggest stone-free rates were lower in
the ESWL group (RR (relative risk) = 0.83, 95% confidence interval [CI] =
0.70–0.98); reflecting this retreatment, rates for ESWL were higher (RR = 2.78,
95% CI = 0.53–14.71) but these findings are associated with much uncertainty.
Complications were less frequent after ESWL (RR = 0.44, 95% CI = 0.21–0.92) and
this option was associated with a shorter hospital stay (mean
difference = 2.10 days, 95% CI = – 2.55 – – 1.64 days). The review
concluded that ureteroscopic treatment of stones was associated with a higher
stone free rate but a higher morbidity (complication rate) and a longer
hospital stay. However, the overall quality of the studies was poor and
inclusion criteria were strict in each study, limiting both the
generalisability and applicability of the review findings. There was limited
evidence on which to judge the comparative effectiveness in clinically
important prognostic subgroups for example location of stones in the ureter.
None of the studies reported on health-related quality of life and only one
reported a cost-effectiveness outcome. The review authors recommended that a
large-scale multicentre RCT was needed to adequately address the effectiveness
and cost-effectiveness of ureteroscopy versus ESWL. A 2011 update of the
Cochrane review [5] has
included two further studies but these have not altered the previous
conclusions.
The European Association of Urology and the
American Urological Association (EAU-AUA) Clinical Guideline Panel on the
management of ureteric stones also conducted a review and meta-analysis
reporting clinical outcomes and complications following treatment of ureteric
stones with ESWL or ureteroscopy, including data from non-randomised
comparisons and case series [4].
Pre-defined outcome measures were stone-free rate and number of additional
procedures required. The results were stratified according to stone location in
the ureter (proximal, mid, distal) and stone diameter (≤ 10 mm,
> 10 mm). All forms of ESWL were analysed as a single treatment
modality in the meta-analysis. The Panel concluded that the main advantage of
ureteroscopy is a higher stone-free rate with a single procedure, but with a
higher complication rate. However, the evidence was insufficient for the Panel
to recommend between ESWL and ureteroscopy and concluded that for patients
requiring active stone removal, either treatment modality is acceptable as
first-line options. For the individual patient, the choice is often determined
by a number of factors including the availability of resources, preference of
the treating urologist, and preference of the patient. The review highlighted
design and reporting deficiencies from available studies, including poor
definition of stone size, inconsistent reporting of outcomes and lack of
randomisation. One of the main recommendations of the Panel was the need to
conduct RCTs comparing the clinical and cost-effectiveness of ESWL and
ureteroscopy.
The aim of this study is to determine whether
in adults with ureteric stones judged to require active treatment, ESWL is not
inferior, clinically, and is more cost-effective compared to
ureteroscopic treatment as the initial management option. AIM
To assess feasibility and efficacy of ESWL for
management of lower ureteric stones
PRIMARY OBJECTIVES
- Stone free rates at 1 week, 8 weeks and 3
months post intervention in both groups
- Acceptability and patient satisfaction of
received procedure at eight weeks post enrollment.
SECONDARY OBJECTIVES
- Additional interventions required up to three
months post primary intervention.
- Complications observed in both groups up to
three months post intervention.
- Acceptability and patient satisfaction of
received procedure at eight weeks post enrollment.
- Loss
of working days for the management of the lower ureteric calculus.
- Pain intensity and analgesic requirement at pre
intervention, during intervention, at one week post intervention and at
eight weeks post enrollment.
- Functional generic health and wellbeing
(SF-12), at eight weeks and at three months post enrollment.
MATERIALS
AND METHODS
Study design: Randomized control trial
Time Duration: January 2023 to December 2024, 24 months
Venue of Study: Department of Urology, All India Institute of Medical Sciences, Jodhpur,
Rajasthan, India.
Study population: Patients with lower ureteric calculus
attending Department of Urology, AIIMS, Jodhpur for management.
PATIENT SELECTION:
INCLUSION
CRITERIA
1.
Presence of lower ureteric stone confirmed by CT KUB
2.
Patients with a ureteric stone requiring active intervention
3.
Adults aged ≥ 18 years
4.
Suitable for either ESWL or ureteroscopic treatment
EXCLUSION CRITERIA:
- Patients who are unable to provide consent
2. Radiolucent stones
3. Active urinary tract infections
4. Pregnancy
5. Uncontrolled hypertension
6. Uncontrolled bleeding tendencies
7. Severe skeletal malformations
8. Vascular malformations within the vicinity of the
stone (such as iliac artery aneurysms)
9. Unable to assume the appropriate position (prone or
supine) for ESWL
10. Solitary kidneys
11. Transplanted kidneys
|