Trial · NCT07896031
BDSF Vs DHS With Anterotational Screw in Vertical FNF
NCT07896031, Phase 2, Active not recruiting, Ain Shams University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. BDSF Vs DHS With Anterotational Screw in Vertical FNF. Trials, record NCT07896031. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896031
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- BDSF Vs DHS With Anterotational Screw in Vertical FNF
- NCT number
- NCT07896031
- Status
- Active not recruiting
- Phases
- Phase 2
- Enrollment
- 30 participants, actual
- Lead sponsor
- Ain Shams University
- Conditions
- Evaluation of BDSF in FNF
- Interventions
- Dynamic Hip Screw with Anterotation Screw Fixation, Biplane Double-Supported Screw Fixation
- 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 | Rates of nonunion | up to 1 year postoperative | Nonunion will be assessed using serial anteroposterior and lateral hip radiographs. It will be defined as failure of fracture healing with a persistent fracture line and absence of progressive trabecular or cortical bridging across the fracture site, with or without persistent pain during weight bearing, at 9 months after fixation. Cases requiring revision surgery for failure of fracture healing before the 9-month assessment will also be classified as nonunion. Radiographs will be independently evaluated by two orthopedic surgeons, with disagreements resolved by consensus. The nonunion rate will be calculated as the number of patients meeting the nonunion criteria divided by the total number of evaluable patients, multiplied by 100. |
| Primary | Functional outcome assessed using the Harris Hip Score was evaluated and calculated at each follow-up visit, with the mean value presented | At 3, 6, and 12 months after surgery. | Hip function will be evaluated using the Harris Hip Score (HHS), which assesses pain, function, absence of deformity, and hip range of motion. The total score ranges from 0 to 100 points, with higher scores indicating better hip function. Results will be classified as excellent (90-100), good (80-89), fair (70-79), or poor (\<70). The mean HHS and the proportion of patients within each functional category will be reported. |
| Primary | Rate of osteonecrosis of the femoral head | Up to 12 months after surgery. | Osteonecrosis of the femoral head will be assessed using serial anteroposterior and lateral hip radiographs. Diagnosis will be based on the development of characteristic radiographic changes, including femoral head sclerosis, cystic changes, subchondral collapse, crescent sign, or loss of femoral head sphericity. Magnetic resonance imaging will be performed when osteonecrosis is clinically suspected but not confirmed on plain radiographs. Osteonecrosis will be classified according to the Association Research Circulation Osseous (ARCO) classification. Patients who undergo revision surgery or conversion to hip arthroplasty because of osteonecrosis will be considered to have reached the outcome. The osteonecrosis rate will be calculated as the number of patients diagnosed with osteonecrosis divided by the total number of evaluable patients, multiplied by 100. |
| Secondary | Mean Operative Time | It was calculated intra-operative | The mean operation time was calculated and compared between the two study groups |
| Secondary | Mean Intraoperative Blood Loss | Up to 4 days postoperative | The mean blood loss was calculated and compared between the two study groups; it was measured intraoperatively and postoperative from suction drains |
| Secondary | Need For Another Operations' Rate | Through study completion, an average of 1 year postoperative | The need for another operation was observed and compared between the two study groups |
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.
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/NCT07896031
GET https://conductscience.org/api/trials/v1/NCT07896031/registered