| CTRI Number |
CTRI/2025/12/099673 [Registered on: 22/12/2025] Trial Registered Prospectively |
| Last Modified On: |
21/12/2025 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Surgical/Anesthesia |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
A RCT to compare outcomes between conventional suture technique vs new technique using dHUC in flexor tendon injury of hand |
|
Scientific Title of Study
|
A randomized control study to compare functional outcomes between
conventional vs newer technique using dHUC in flexor tendon injuries of the hand |
| 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 Mrthyunjayani Sharma |
| Designation |
Acadenic senior resident |
| Affiliation |
ALL INDIA INSTITUE OF MEDICAL SCIENCES, JODHPUR |
| Address |
Department of Burns and Plastic Surgery , AIIMS jodhpur , heavy industrial area, Basni, Jodhpur
Jodhpur RAJASTHAN 342001 India |
| Phone |
9094258896 |
| Fax |
|
| Email |
mrthyunjayani96@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Prakash Chandra Kala |
| Designation |
Additional professor |
| Affiliation |
ALL INDIA INSTITUE OF MEDICAL SCIENCES, JODHPUR |
| Address |
Department of Burns and Plastic Surgery , AIIMS jodhpur , heavy industrial area, Basni, Jodhpur
Jodhpur RAJASTHAN 3420021 India |
| Phone |
8460952204 |
| Fax |
|
| Email |
drpckala@gmail.com |
|
Details of Contact Person Public Query
|
| Name |
Dr Prakash Chandra kala |
| Designation |
Additional professor |
| Affiliation |
ALL INDIA INSITITUE OF MEDICAL SCIENCES, JODHPUR |
| Address |
Department of Burns and Plastic surgery , AIIMS jodhpur , heavy industrial area, Basni, Jodhpur
Jodhpur RAJASTHAN 342001 India |
| Phone |
8460952204 |
| Fax |
|
| Email |
drpckala@gmail.com |
|
|
Source of Monetary or Material Support
|
|
|
Primary Sponsor
|
| Name |
ALL INDIA INSTIUTE OF MEDICAL SCIENCES JODHPUR |
| Address |
Department of Burns and Plastic Surgery , AIIMS , Jodhpur, heavy industrial area , Basni, Jodhpur 342001 |
| 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 |
| DrMrthyunjayani Sharma |
All India Institue Of Medical Sciences , Jodhpur |
Department of Burns and Plastic Surgery,Heavy industrial area, Basni, Jodhpur Jodhpur RAJASTHAN |
9094258896
mrthyunjayani96@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| INSTITUTIONAL ETHICS COMMITEE (CLINICAL TRIAL) |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: S661||Injury of flexor muscle, fascia and tendon of other and unspecified finger at wrist and hand level, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Comparator Agent |
conventional suture repair |
conventional repair of flexor tendon injury using the modified kessler technique, al repair site
both the comparator agent group and control group will have the same post-operative period monitoring , physiotherapy ( kleinert protocol) and wound care protocols
assessment of post operative results will be done as per the mentioned criteria and time intervals in primary and secondary outcomes |
| Intervention |
dHUC membrane |
post conventional repair of flexor tendon injury using the modified kessler technique, sterile dHUC membrane is to be wrapped around the surgical repair site at the time of surgery only after which both the comparator agent group and control group will have the same post operative period monitoring (kleinert protocol ) , physiotherapy and wound care protocols assessment of post operative results will be done as per the mentioned criteria and time intervals in primary and secondary outcomes |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
99.00 Year(s) |
| Gender |
Both |
| Details |
Consenting adults with injuries of flexor tendons involving 2 or more digits
(index, middle, ring, and little finger) of the hand. |
|
| ExclusionCriteria |
| Details |
Associated fractures requiring stabilization
Tendon injury concomitant with flap or graft coverage
Associated digital nerve repair
Co-existing myopathies
Joint contracture/ deformity
Collagen vascular disease/ connective tissue disorder |
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
Other |
|
Blinding/Masking
|
Participant and Outcome Assessor Blinded |
|
Primary Outcome
|
| Outcome |
TimePoints |
| to assess the functional outcomes of application of dHUC ( dehydrated human umblical cord ) membrane and conventional repair vs conventional repair in flexor tendon injuries of hand at 3 months and 6 months post repair |
to assess the functional outcomes of application of dHUC ( dehydrated human umblical cord ) membrane and conventional repair vs conventional repair in flexor tendon injuries of hand at 3 months and 6 months post repair |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| incidence of surgical site infection upto 1 month post surgery |
1 month post surgery |
| evaluation of overall function & disability using patient reported outcome using qDASH questionnaire for overall hand function & disability at 3 & 6 months after surgery |
3 months & 6 months post surgery |
| assessment of grip strength using Jamar gauge at 3 months & 6 months post surgery |
3 months annd 6 months post surgery |
| loss of working days post injury ( days away from work) at end of 6 months |
6 months post surgery |
| disability evaluation of upper limb in accordance with the gazette of India issued by ministry of social justice & empowerment in year 2024 at 6 months post repair |
6 months post surgery |
|
|
Target Sample Size
|
Total Sample Size="30" Sample Size from India="30"
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)
|
05/01/2026 |
| 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="1" Months="6" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Open to Recruitment |
|
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
|
Research hypothesis We hypothesize that in adult patients undergoing surgical repair for flexor tendon injuries of the hand, the newer technique with sterile dehydrated human umbilical cord- derived membrane (dHUC) is associated with significantly improved functional outcomes and enhanced tendon healing compared to conventional repair techniques. Null hypothesis We hypothesize that in adult patients undergoing surgical repair for flexor tendon injuries of the hand, the newer technique with sterile dehydrated human umbilical cord- derived membrane (dHUC) does not significantly improve functional outcomes compared to conventional repair techniques Aim This study aims to evaluate the effectiveness of newer technique with dehydrated umbilical cord compared to conventional tendon repair in improving the functional outcomes in adult patients with flexor tendon injuries of the hand. Primary objective To assess the functional outcomes of application of d-HUC and conventional repair vs conventional repair in flexor tendon injuries of the hand at 3 months and 6 months post-repair Secondary objectives 1 Incidence of surgical site infection up to 1-month post-surgery. 2 Evaluation of overall hand function and disability using patient-reported outcomes using the Quick Disabilities of the Arm, Shoulder, and Hand (Quick DASH) questionnaire for overall hand function and disability at 3 and 6 months after surgery. 3 Assessment of grip test using Jamar gauge at 3- and 6-months post-surgery. 4 Loss of working days post injury (days away from work) at the end of 6 months. 5 Disability evaluation of the upper limb in accordance with The Gazette of India issued by the Ministry of Social Justice and Empowerment in the year 2024 at 6 months post repair.
Expected outcome 1 Reduced inflammation and adhesions with improved tendon gliding 2 Improved functional outcome post-flexor tendon injury repair 3 Early return to work
Novelty Statement: Paucity of literature on the usage of dehydrated umbilical cord derivative membrane in flexor tendon injury of the hand Unlike traditional repair techniques that rely solely on mechanical strength and are often complicated by postoperative adhesions and restricted motion, the dHUC membrane offers several innovative advantages which include physical barrier to adhesion formation, rich array of growth factors, cytokines, hyaluronic acid, and extracellular matrix proteins, which facilitate cellular proliferation, angiogenesis, and may enhance tissue remodelling at the repair site. Rationale of the study Given the tendons complex architecture, vital function in the hand, and high risk of postoperative sequelae such adhesion development and reduced tendon gliding, flexor tendon injuries pose a substantial challenge to hand surgeons. Achieving the best possible functional results is still challenging, even with advancements in surgical procedures and postoperative rehabilitation. The key objective of traditional repair techniques is to mechanically restore tendon continuity. They frequently overlook the biological context necessary for the best possible healing, though. Fibroblastic activity usually impedes the healing process by causing peritendinous adhesions that restrict range of motion and functional recovery.Biologic scaffolds are new tissue engineering advancements that may be used as tendons’ repair adjuncts. Sterile dehydrated human umbilical cord-derived membrane (dHUC), which is abundant in growth factors, anti-inflammatory cytokines, and extracellular matrix components, is one such substance. These characteristics could enhance clinical results by minimizing adhesion formation, promoting regenerative repair, and lowering inflammation. The effectiveness of dHUC in treating flexor tendon injuries is yet unknown, despite research showing encouraging outcomes in various orthopedic and soft tissue applications .In order to produce high-quality evidence about its usefulness, safety, and cost- effectiveness in comparison to conventional surgical repair, a thorough evaluation in a double-blinded randomized controlled trial(RCT) setting is necessary. |