Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
NCT06267105

A Clinical Study to Compare Functional Outcomes After Surgery Using a Transverse or Longitudinal Surgical Incision in the Skin.

Led by Corporacion Parc Tauli · Updated on 2024-08-15

36

Participants Needed

1

Research Sites

41 weeks

Total Duration

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AI-Summary

What this Trial Is About

Trigger finger is a common pathology in the hand. Patients suffer from pain and depending on which tasks, patients have difficulty to perform them. Its treatment in initial and less serious phases includes conservative measures, but failure of these may require releasing the trigger finger with surgery. The surgical technique performed for trigger finger is the opening of the A1 pulley, the skin incisions used for this surgery are various (transverse, longitudinal, oblique). Trigger finger surgery presents good results in terms of resolution, but complications may also occur. The reason for this study is to assess whether there are functional differences using the Dash scale when we perform a transverse or longitudinal incision in trigger finger surgery.

CONDITIONS

Official Title

A Clinical Study to Compare Functional Outcomes After Surgery Using a Transverse or Longitudinal Surgical Incision in the Skin.

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 18 years of age.
  • Clinical diagnosis of trigger finger grade II to IV.
Not Eligible

You will not qualify if you...

  • Thumb involvement.
  • Multiple fingers affected (polydigital).
  • Allergy to local anesthetics and/or vasoconstrictor agents.
  • Previous surgery on the affected finger.
  • Patients considered unsuitable by the researcher due to inability to comply with follow-up, comorbidities, poor physical or mental health, or substance abuse.

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Hospital Parc taulí

Sabadell, Barcelona, Spain, 08208

Actively Recruiting

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Research Team

M

Mireia Vinas

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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