Trial · NCT07894718
Effect of Ultrasound-Guided Posterior Cutaneous Nerve of the Forearm Epicondylar Branch Block on Pain and Function in Lateral Epicondylitis (PCNF-BrEpi)
NCT07894718, Not applicable, Recruiting, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Ultrasound-Guided Posterior Cutaneous Nerve of the Forearm Epicondylar Branch Block on Pain and Function in Lateral Epicondylitis (PCNF-BrEpi). Trials, record NCT07894718. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07894718
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Ultrasound-Guided Posterior Cutaneous Nerve of the Forearm Epicondylar Branch Block on Pain and Function in Lateral Epicondylitis (PCNF-BrEpi)
- NCT number
- NCT07894718
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 84 participants, estimated
- Lead sponsor
- Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
- Conditions
- Lateral Epicondylitis
- Interventions
- Ultrasound-guided triamcinolone injection, Ultrasound-guided PCNF-BrEpi block, Conventional therapy (home exercise program and epicondylitis band)
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Patient-Rated Tennis Elbow Evaluation (PRTEE) | At baseline, 1 month, and 3 months after treatment initiation | PRTEE is a patient-reported outcome measure used to assess pain and functional disability related to tennis elbow. |
| Secondary | Visual Analog Scale | At baseline, 1 month, and 3 months after treatment initiation | Visual Analog Scale used to assess pain intensity. |
| Secondary | Quick Disabilities of the Arm, Shoulder and Hand(QuickDASH) | At baseline, 1 month, and 3 months after treatment initiation | QuickDASH is a patient-reported outcome measure used to assess upper extremity physical function and symptoms. |
| Secondary | Common Extensor Tendon Thickness Measured by Ultrasonography | At baseline, 1 month, and 3 months after treatment initiation | Thickness of the common extensor tendon measured by ultrasonography. |
| Secondary | Hand Grip Strength Measured by Dynamometry | At baseline, 1 month, and 3 months after treatment initiation | Hand grip strength measured using a hand dynamometer. |
| Secondary | Global Rating of Treatment Outcome | At baseline, 1 month, and 3 months after treatment initiation | Patient's global assessment of the overall treatment outcome. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers5
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07894718
GET https://conductscience.org/api/trials/v1/NCT07894718/registered