Trial · NCT07885280
Comparing Surgical and Nonsurgical Outcomes of Tennis Elbow
NCT07885280, Not applicable, Not yet recruiting, University of Pittsburgh
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparing Surgical and Nonsurgical Outcomes of Tennis Elbow. Trials, record NCT07885280. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07885280
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparing Surgical and Nonsurgical Outcomes of Tennis Elbow
- NCT number
- NCT07885280
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 200 participants, estimated
- Lead sponsor
- University of Pittsburgh
- Conditions
- Lateral Epicondylitis
- Interventions
- Conservative Arm, Surgical
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Patient-Rated Tennis Elbow Evaluation (PRTEE) from baseline to 1 year | Baseline, 6 weeks, 3 months, 6 months, 1 year | 0 indicates no pain and no disability; 100 indicates worst imaginable pain and significant functional deficit; "change" refers to differences between each timepoint and the baseline, as well as the differences between each consecutive timepoint |
| Secondary | Change in Patient-Rated Tennis Elbow Evaluation (PRTEE) at All Other Timepoints | Baseline, 6 weeks, 3 months, 6 months, 1 year, 2 years | 0 indicates no pain and no disability; 100 indicates worst imaginable pain and significant functional deficit; "change" refers to differences between each timepoint and the baseline, as well as the differences between each consecutive timepoint |
| Secondary | Change in Quick Disabilities of the Arm, Shoulder, and Hand (QuickDASH) at Each Timepoint; "change" refers to differences between each timepoint and the baseline, as well as the differences between each consecutive timepoint | Baseline, 6 weeks, 3 months, 6 months, 1 year, 2 years | 0 indicates no disability; 100 indicates the most severe disability; "change" refers to differences between each timepoint and the baseline, as well as the differences between each consecutive timepoint |
| Secondary | Grip Strength | Baseline, 6 weeks, 3 months, 6 months, 1 year, 2 years | Change in grip strength (in pounds and kilograms) at 90 degrees of elbow flexion, and at full elbow flexion; "change" refers to differences between each timepoint and the baseline, as well as the differences between each consecutive timepoint |
| Secondary | Conversion Rate | Baseline to 2 years after baseline | Rate of conversion to surgery (as a percentage) |
| Secondary | Patient Satisfaction (5-Point Likert Scale) | Baseline, 6 weeks, 3 months, 6 months, 1 year, 2 years | Participant-reported satisfaction with treatment outcome using a 5-point Likert scale (minimum 1; maximum 5; higher score indicates greater satisfaction) |
| Secondary | Global Rating of Change | Baseline, 6 weeks, 3 months, 6 months, 1 year, 2 years | Participant-reported overall change in symptoms and function (minimum -3 indicating much worse; maximum +3 indicating much better) |
| Secondary | Return to Work/Activities (Self-Reported Work Status) | Baseline to 2 years after baseline | Time, in days, from enrollment (or from surgery, for the surgical arm and crossovers) to return to work, based on participant self-reported work status (working, modified duty, or off work due to symptoms), and to participant-reported return to full activity or sport. |
| Secondary | Complication Rates | 1 year post-op | |
| Secondary | Reoperation Rate | 1 year post-op |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT07885280
GET https://conductscience.org/api/trials/v1/NCT07885280/registered