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Trial · NCT07907159

Hybrid Closed Wedge High Tibial Osteotomy

NCT07907159, Not applicable, Not yet recruiting, Assiut University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Hybrid Closed Wedge High Tibial Osteotomy. Trials, record NCT07907159. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07907159

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Hybrid Closed Wedge High Tibial Osteotomy
NCT number
NCT07907159
Status
Not yet recruiting
Phases
Not applicable
Enrollment
20 participants, estimated
Lead sponsor
Assiut University
Conditions
Patello-femoral Osteoarthritis
Interventions
Hybrid Closed Wedge High Tibial Osteotomy
First posted
2026-10-30
Last updated
2026-10-30

Source ClinicalTrials.gov

Registered outcomes3

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryClinical improvement by KOOS Functional knee scorefrom enrollment till 12 months post-operative
Validated knee scoring systems will be recorded preoperatively and during follow-up by Knee injury and Osteoarthritis Outcome Score (KOOS) The standard full-length KOOS consists of 42 items divided into 5 separate subscales: * Pain (9 items) * Other Symptoms (such as swelling, stiffness, and range of motion) (7 items) * Function in Daily Living (ADL) (17 items) * Function in Sport and Recreation (Sport/Rec) (5 items) * Knee-Related Quality of Life (QOL) (4 items Scoring * Format: Patients rate each item using a 5-point Likert scale (from 0 to 4) based on their experiences over the preceding week. * Scale: Each subscale is calculated independently and transformed to a 0 to 100 scale. * Interpretation: * 0 represents extreme knee problems / total disability. * 100 represents no knee problems / perfect joint health. * No Total Score: An aggregate or single total score is not calculated
PrimaryClinical improvement by AKPS Functional knee scorefrom enrollment till 12 months post-operative
Validated knee scoring systems will be recorded preoperatively and during follow-up by Kujala Anterior Knee Pain Scale (AKPS) The AKPS is a 13-item, patient-reported questionnaire used to evaluate subjective symptoms and functional limitations in people with patellofemoral disorders Overview of the Scale * Total Score Range: 0 to 100 points * Interpretation: * 85-100: Near-normal / minimal dysfunction (Excellent) * 70-84: Mild dysfunction (Scores around 70 often reflect moderate disability) * 50-69: Moderate patellofemoral dysfunction (Fair) * 0-49: Severe patellofemoral dysfunction with significant pain and limitations (Poor)
SecondaryMechanical axis correctionfrom enrollment till 12 months post-operativeThe invistigators aim for HKA angle at approximately 0°

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.

Papers6

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
20217394BACKGROUNDPubMed
20305774BACKGROUNDPubMed
20833833BACKGROUNDPubMed
22773067BACKGROUNDPubMed
25008139BACKGROUNDPubMed
26026274BACKGROUNDPubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT07907159

GET https://conductscience.org/api/trials/v1/NCT07907159/registered