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Recruiting NCT06296017

NCT06296017 Effectiveness of Conservative Interventions in the Treatment of Trigger Finger

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Clinical Trial Summary
NCT ID NCT06296017
Status Recruiting
Phase
Sponsor Hacettepe University
Condition Trigger Finger
Study Type INTERVENTIONAL
Enrollment 54 participants
Start Date 2023-10-02
Primary Completion 2026-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Experimental: Extracorporeal Shock Wave TherapyTrigger Finger SplintExtracorporeal Shock Wave Therapy+ Trigger Finger Splint

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 54 participants in total. It began in 2023-10-02 with a primary completion date of 2026-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

There is no study in the literature comparing the effectiveness of ESWT and splint therapy, which are the most commonly used approaches in the treatment of Trigger Finger (TF). The aim in this study is to investigate the effectiveness of ESWT and splint therapy used in the treatment of TF.

Eligibility Criteria

Inclusion Criteria: * Volunteering * Being between the ages of 18-65 * Being diagnosed with stage 1 or stage 2 (according to the Froimson classification) trigger finger * Having the language and cognitive skills to answer the questionnaires used in the evaluation Exclusion Criteria: * Being pregnant * Having an inflammatory disorder * Having had surgery on the hand/wrist * Having a neurological disease * NSAIDs, painkillers, etc. being on medication * De Quervain's tenosynovitis, carpal tunnel syndrome

Contact & Investigator

Central Contact

Feray Karademir

✉ karademirferay@gmail.com

📞 +90 505 313 75 82

Principal Investigator

Kadir ÇEVİK

STUDY DIRECTOR

Etlik Şehir Hastanesi

Frequently Asked Questions

Who can join the NCT06296017 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Trigger Finger. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06296017 currently recruiting?

Yes, NCT06296017 is actively recruiting participants. Contact the research team at karademirferay@gmail.com for enrollment information.

Where is the NCT06296017 trial being conducted?

This trial is being conducted at Ankara, Turkey (Türkiye).

Who is sponsoring the NCT06296017 clinical trial?

NCT06296017 is sponsored by Hacettepe University. The principal investigator is Kadir ÇEVİK at Etlik Şehir Hastanesi. The trial plans to enroll 54 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology