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The Effect of Human Amniotic Membrane Allograft on Functional Recovery After Flexor Tendon Repair

NCT02361814 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2017-06-27

No results posted yet for this study

Summary

The objective of this pilot study is to gain observational insight into potential preventive features of amniotic membrane transplantation in the adhesion formation after flexor tendon repair.

Conditions

  • Flexor Tendon Injury

Interventions

PROCEDURE

The use of amnionic membrane allograft

After the conventional flexor tendon repair, the amniotic membrane will be wrapped around the tendons and its borders will be fixed to the remaining tendon sheath.

Sponsors & Collaborators

  • Tampere University Hospital

    collaborator OTHER

  • Central Finland Hospital District

    collaborator OTHER

  • Tampere University

    lead OTHER

Principal Investigators

  • Harry Göransson, M.D., Ph.D. · Tampere University Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2016-09-30
Completion
2016-09-30

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02361814 on ClinicalTrials.gov