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

Clinical Study to Compare Functional Results in Patients Affected by Trigger Finger When Surgery is Performed Through a Transverse or Longitudinal Surgical Incision in the Skin.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06267105
Enrollment
36
Registered
2024-02-20
Start date
2024-05-15
Completion date
2025-03-31
Last updated
2024-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Functional Disturbance as Result

Brief summary

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.

Interventions

Incision performed longitudinally

PROCEDURETransverse incision

Incision performed transversally

Sponsors

Corporacion Parc Tauli
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Patients over 18 years of age. * Clinical diagnosis of trigger finger grade II to IV. Grade I (pre-trigger) Pain, history of entrapment, but not demonstrable on physical examination, tenderness over the A1 pulley. Grade II (active) Demonstrable entrapment, but the patient can actively extend the finger. Grade III (passive) Demonstrable entrapment, patient requires passive extension IIIA or inability to actively flex IIIB. Grade IV (contracture) Demonstrable entrapment with fixed flexion contracture of the PIP.

Exclusion criteria

* Thumb * Polydigital * Allergy to local anesthetics and/or vasoconstrictor agents. * Previous surgery * Patients who, in the researcher's opinion, are not good candidates for the study (e.g. inability to comply with the follow-up program, comorbidity, poor physical or mental health in general, drug or alcohol abuse problems...).

Design outcomes

Primary

MeasureTime frameDescription
Functional improvement of the patient after surgeryImmediately after surgeryfunctional improvement of the patient after surgery, which will be assessed with the Dash scale, 1 being difficult while 5 being unable

Secondary

MeasureTime frameDescription
Resolution1, 3 and 6 monthsPresence or absence of engagment
Flushed1, 3 and 6 monthsRed or not red
Pain feeling1, 3 and 6 monthsEVA scale from 0 to 10, being 10 a lot of pain
Contracture1, 3 and 6 monthsRange of motion in degrees
Surgeon comfortImmediately after surgeryEcellent, good, poor
Nerve injury1, 3 and 6 monthsAllen test to evaluate correct circulation, the hand should turn white when pressing
Return to work1, 3 and 6 monthsHow many weeks after surgery
Reincorporation to activities1, 3 and 6 monthsHow many weeks after surgery
Sensitivity Test1, 3 and 6 monthsIn a scale from 0 to 10
Infection1, 3 and 6 monthsSeptic signs such the area is red, hot, swelling or has drain pus

Countries

Spain

Contacts

Primary ContactMireia Vinas
mmvinas@tauli.cat+34 93 723 10 10

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026