CTRI Number |
CTRI/2018/01/011229 [Registered on: 10/01/2018] Trial Registered Retrospectively |
Last Modified On: |
09/01/2018 |
Post Graduate Thesis |
No |
Type of Trial |
Interventional |
Type of Study
|
Surgical/Anesthesia |
Study Design |
Randomized, Parallel Group, Active Controlled Trial |
Public Title of Study
|
Study on the effect of combination of pain killers on pain relief during and after the surgery |
Scientific Title of Study
|
Effect of multimodal perioperative analgesia on stress response to surgery and on post-operative pain score |
Trial Acronym |
|
Secondary IDs if Any
|
Secondary ID |
Identifier |
NIL |
NIL |
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
Name |
Dr Savitha K S |
Designation |
Professor |
Affiliation |
St Johns Medical College & Hospital |
Address |
Department of Anaesthesia
St John’s Medical College & Hospital
Sarjapur Road
Koramangala
Bangalore
Bangalore KARNATAKA 560034 India |
Phone |
9844638121 |
Fax |
0 |
Email |
drsavitha_ks@yahoo.com |
|
Details of Contact Person Scientific Query
|
Name |
Dr Savitha K S |
Designation |
Professor |
Affiliation |
St Johns Medical College & Hospital |
Address |
Department of Anaesthesia
St John’s Medical College & Hospital
Sarjapur Road
Koramangala
Bangalore
Bangalore KARNATAKA 560034 India |
Phone |
9844638121 |
Fax |
0 |
Email |
drsavitha_ks@yahoo.com |
|
Details of Contact Person Public Query
|
Name |
Dr Savitha K S |
Designation |
Professor |
Affiliation |
St Johns Medical College & Hospital |
Address |
Department of Anaesthesia
St John’s Medical College & Hospital
Sarjapur Road
Koramangala
Bangalore
Bangalore KARNATAKA 560034 India |
Phone |
9844638121 |
Fax |
0 |
Email |
drsavitha_ks@yahoo.com |
|
Source of Monetary or Material Support
|
St John’s Medical College & Hospital
Department of Anaesthesia
Sarjapur Road
Koramangala
Bangalore-560034
|
|
Primary Sponsor
|
Name |
Dr Savitha K S |
Address |
Department of Anaesthesia
St John’s Medical College & Hospital
Sarjapur Road
Koramangala
Bangalore
|
Type of Sponsor |
Other [Self] |
|
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 Savitha K S |
St John’s Medical College & Hospital |
Department of Anaesthesia
Bangalore KARNATAKA |
9844638121 0 drsavitha_ks@yahoo.com |
|
Details of Ethics Committee
|
No of Ethics Committees= 1 |
Name of Committee |
Approval Status |
institutional Ethical Review board |
Approved |
|
Regulatory Clearance Status from DCGI
|
|
Health Condition / Problems Studied
|
Health Type |
Condition |
Patients |
American Society of Anapatientsesthesiologists Class I and II , |
|
Intervention / Comparator Agent
|
Type |
Name |
Details |
Intervention |
Group A: (MMA group/study group) |
Received intravenous diclofenac sodium 75mg, paracetamol 1gm, and clonidine 0.75µg/kg, and local infiltration 20ml (bupivacaine 0.25% with adrenaline 1:1000) as analgesics in multimodal regime |
Comparator Agent |
Group B: (Conventional regime group/control group) |
Received intravenous paracetamol 1gm and local infiltration 20ml (saline with adrenaline). |
|
Inclusion Criteria
|
Age From |
20.00 Year(s) |
Age To |
65.00 Year(s) |
Gender |
Both |
Details |
1. Both sexes
2. BMI (Body Mass Index) 18 to 30
3. Patients undergoing lumbar spine surgery
4. ASA physical status I and II
|
|
ExclusionCriteria |
Details |
1. Pregnant women
2. Patients with bronchial asthma
3. Patients with history of drug allergy.
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
Method of Concealment
|
An Open list of random numbers |
Blinding/Masking
|
Participant and Investigator Blinded |
Primary Outcome
|
Outcome |
TimePoints |
To assess the difference in serum cortisol and random blood sugar between MMA regime and the conventional analgesic regime in patients undergoing lumbar spine surgery. |
Two blood samples were drawn; one just before tracheal tube placement and another one 30 min following skin incision for random serum cortisol and random blood sugar. |
|
Secondary Outcome
|
Outcome |
TimePoints |
To compare post extubation sedation and visual analogue score (VAS) between the two groups. |
Post operative sedation and pain score were assessed at 5min and 30min post-extubation respectively. |
To compare the incidence of adverse effects (perioperatively:bradicardia and bronchospasm, postoperatively: respiratory depression, nausea and vomiting ) between the two groups. |
Bradicardia and bronchospasm were looked after administration of of each drug preoperatively and throught the surgery. Respiratory depression, nausea and vomiting were looked for in the postoperative period |
|
Target Sample Size
|
Total Sample Size="42" Sample Size from India="42"
Final Enrollment numbers achieved (Total)= "42"
Final Enrollment numbers achieved (India)="42" |
Phase of Trial
|
Phase 2 |
Date of First Enrollment (India)
|
15/06/2011 |
Date of Study Completion (India) |
29/05/2015 |
Date of First Enrollment (Global) |
Date Missing |
Date of Study Completion (Global) |
Date Missing |
Estimated Duration of Trial
|
Years="4" Months="0" Days="0" |
Recruitment Status of Trial (Global)
|
Not Applicable |
Recruitment Status of Trial (India) |
Completed |
Publication Details
|
Not yet published |
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
|
Brief Summary
|
Effect of multimodal perioperative analgesia on stress response to surgery and on post-operative pain score Introduction Management of acute pain gained importance in the early 1930s. Even after eight decades, the incidence of postoperative pain is 75%. Pre-emptive multimodal analgesia (MMA) can be effective in preventing and treating acute pain. Pre-emptive analgesia is an evolving concept where analgesics are timed to prevent establishment of central sensitization. The concept of MMA was pioneered by Prof Henrik Kehlet in early 1990s. In MMA all the four elements of the pain processing pathway (1.Transduction, 2.Transmission, 3.Modulation and 4.Perception) are targeted with drugs having different mechanism of actions for clinically measurable pain relief. Aim of the study was to assess the effect of MMA on random serum cortisol, random blood sugar, propofol requirement for induction, and to compare post extubation sedation and visual analog scale score between the two groups. Materials and methods After obtaining Institutional Review Board approval and Informed written consent, a prospective, double blind, randomized clinical trial involving 42 patients belonging to the American Society of Anaesthesiologists Class I and II scheduled to undergo elective lumbar spine surgery were allocated into two groups of 21 each. Study group received injection diclofenac sodium, paracetamol, clonidine, and skin infiltration with bupivacaine adrenaline and Control group received paracetamol and skin infiltration with saline adrenaline. Analgesics were administered as per their onset of action, providing adequate time for their clinical effects. BIS guided induction was done with incremental doses of injection propofol. Two blood samples were drawn; one just before tracheal tube placement and another one 30 min following skin incision for random serum cortisol and random blood sugar. Post operative sedation and pain score were assessed at 5min and 30min post-extubation respectively. Patients with moderate pain received rescue analgesic pethidine 0.5-1mg/kg. Statistical Methods: Statistical significance of mean difference between the two groups was analyzed using Independent t-test and within group using paired t-test. Repeated Measure Analysis of Variance (RMANOVA) was used to compare the outcomes between the groups with change over time. All the categorical data between groups were compared using Chi square test. The data that was not normally distributed were compared between the groups using Mann-Whitney U test. p<0.05 was considered statistically significant. Results Random serum cortisol (Table-1), random blood sugar (Table-1) and postoperative sedation score between the groups were comparable. Induction dose of propofol was significantly low in MMA group (Table-2). In the MMA group 100% patients had mild pain whereas in the control group 85.7% of the patients had moderate pain (Table-3) where rescue analgesic was administered. No side effects were noted in the study group. Conclusion As a response to tissue injury, inflammatory mediators are released irrespective of analgesics administered, but the response to painful stimuli depends on the intensity of analgesia. With pre-emptive MMA nociceptors at all levels of pain processing are primed with analgesics, which inhibits nociception and ensures intense analgesia with narcosis and potentiates the clinical efficacy of induction drugs with minimal adverse effects. |