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TerminatedNCT02461680FLEXORUpdated Aug 21, 2019

Treatment for Partial Lesions of the Fingers Flexor Tendons : Tangential Resection or Direct Suture

An interventional study of tangential resection and suture in Flexor Tendon Injury and Lesions Of The Fingers Flexor Tendons, sponsored by University Hospital, Strasbourg, France. Terminated at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-08-21.

Sponsored by University Hospital, Strasbourg, France · Not applicable, Interventional, and Treatment

Why this study was terminated
recruitment difficulty
Phase
Not applicable
Study type
Interventional
Enrollment
3
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Flexors tendon injuries are frequent and serious with a potential of definitive functional aftereffects. In the case of partial injury, the treatment is debated. There are 2 techniques of possible repair, the direct suture and the tangential resection. The investigators have already demonstrated that this last technique was favorable for injuries going to 50 %. In the case of partial section between 50 and 75 %, the investigators think that the technique of tangential resection compared with the direct suture would not increase the risks of secondary breaks, would authorize even an immediate mobilization and would decrease the secondary complications.

The main objective is to highlight that the tangential resection is not lower than the classic technique on the clinical plan The secondary objectives are to highlight the non-inferiority of the tangential technique in clinical terms (pains, dexterity, complications), radiologics (MRI, ultrasound) and functional (function, go back to leisures and professional activities)

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Conditions studied

  • Flexor Tendon Injury
  • Lesions Of The Fingers Flexor Tendons

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Keywords

  • partial section of the flexor tendons
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In context

Tendon Injuries

92 studies on the registry are indexed under Tendon Injuries; 15 are open to participants now.

This study's enrollment of 3 is below the median of 40 across 64 interventional studies indexed under Tendon Injuries.

Browse Tendon Injuries studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 966 studies on the registry; 342 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • wound dating less than 48 hours
  • partial section from 50 % to 75 % of the flexor tendons (deep and/or superficial flexors, long flexor of the thumb) in zones 1, 2, 3, T1 and T2
  • tendinous injuries on a single finger

Exclusion criteria

Exclusion Criteria:

-

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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
3 participants (actual)

Study arms

  • Experimental
    Tangential resection

    the tendon's injury is treated with a tangential resection

    Procedure: tangential resection

  • Active comparator
    Suture

    The tendon's injury is sutured

    Procedure: suture

Interventions

  • Proceduretangential resection

    the tendon's injury is treated with a tangential resection performed with a surgical blade N°11 The shape of the tangential resection was adapted such that the cross-section disappered

  • Proceduresuture
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What researchers measure

Primary outcomes

  1. Total active motion Grasp

    Total active motion is the addition of angles in flexion of IPP, IPD and MCP joints of a finger in active mobility

    Time frame: third month,

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Study locations

1 site
  • CHU Strasbourg,
    Strasbourg, 67000, France
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02461680
Lead sponsor
University Hospital, Strasbourg, France
Responsible party
Sponsor
First posted
Jun 3, 2015
Start date
Feb 2016
Primary completion
Feb 2019
Completion
Feb 2019
Last update
Aug 21, 2019

Study contacts

Sybille FACCA, MD
principal investigator · CHU Strasbourg

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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