Adjuvant Versus Neo-adjuvant Radiotherapy in Patients With Resectable Soft Tissue Sarcoma in Extremities : Wound Complications
NCT ID: NCT05442333
Last Updated: 2023-05-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
20 participants
INTERVENTIONAL
2021-09-01
2023-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Post-operative Radiotherapy in Poor Responders Ewing's Sarcoma Patients
NCT01734863
Radiation Therapy Before Surgery for Localized, Resectable Soft Tissue Sarcoma of the Extremity and Superficial Trunk
NCT04562480
Safety and Efficacy of Preoperative SBRT and Radical Surgery for Soft Tissue Sarcoma of Extremities
NCT06760221
Preoperative Radiotherapy for Sarcomas of the Extremities With Intensity-Modulation, Image-Guidance and Small Safety-margins
NCT01552239
The Total Neoadjuvant Therapy for Soft Tissue Sarcoma of the Extremities
NCT06593899
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Primary (Preoperative) Diagnosis and Evaluation
Clinical Evaluation. History. General examination. Local examination.
Radiological Evaluation:
Plain X-ray for the affected limb to determine presence of any bone affection or invasion.
Preoperative MRI scan to determine the extent of soft tissue, bone and neurovascular bundle invasion.
Preoperative bone scan to determine skeletal metastatic load.
Perioperative protocol:
Preoperative radiotherapy 3-6 weeks before surgical excision. Postoperative radiotherapy 3- 6 weeks or more after surgical excision Tissue diagnosis will be obtained.
Operative management:
Surgical excision of whole tumour with wide safety margin.
Data collection:
Patient demographics (age, sex). Activity level Primary sarcoma type Patient comorbidities Timing of Preoperative radiotherapy if present. Timing of Postoperative radiotherapy if present. Time from diagnosis to surgery. recurrence Operative time (minutes) measured from skin incision to wound closure. Follow up regarding wound complications, local recurrence or infection. local recurrence will be followed up till the end of the study
Follow up strategy:
The patients with preoperative radiotherapy:
will be assessed 2 weeks postoperative regarding wound signs of infection (redness, hotness or discharge).
1 month postoperatively for wound complete closure and exclude signs of infection.
3 months postoperatively for wound dehiscence, swelling or local recurrence. 6 months postoperatively for local recurrence, pathological fractures or joint stiffness
The patients with postoperative radiotherapy:
will be assessed 3 weeks post radiation regarding wound signs of infection (redness, hotness or discharge).
6 weeks post radiation for wound dehiscence 3 months post radiation for local swelling or recurrence 6 months post radiation for local recurrence, joint stiffness or pathological fractures.
Statistical Analysis: Statistical package for social science (SPSS 15.0.1 for windows ; 〖SPSS Inc,Chicago,IL,2001). Data will be presented as Mean and Standard deviation ( +/-SD) for quantitative parametric data , and Median and Interquartile range for quantitative non parametric data. Frequency and percentage will be used for presenting qualitative data. Suitable analysis will be done according to the type of data obtained. P\<0.05 will be considered significant.
Statistical Package: data entry and statistical analysis of the collected data will be performed using reliable software program.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
preoperative radiotherapy
The patients which will receive preoperative radiotherapy
surgical resection with safety margin
• The patients with preoperative radiotherapy:
1. will be assessed 3 weeks post radiation regarding wound signs of infection (redness, hotness or discharge).
2. 6 weeks post radiation for wound dehiscence
3. 3 months post radiation for local swelling or recurrence
4. 6 months post radiation for local recurrence, joint stiffness or pathological fractures.
The patients with postoperative radiotherapy:
1. will be assessed 3 weeks post radiation regarding wound signs of infection (redness, hotness or discharge).
2. 6 weeks post radiation for wound dehiscence
3. 3 months post radiation for local swelling or recurrence
4. 6 months post radiation for local recurrence, joint stiffness or pathological fractures.
postoperative radiotherapy
The patients which will receive postoperative radiotherapy
surgical resection with safety margin
• The patients with preoperative radiotherapy:
1. will be assessed 3 weeks post radiation regarding wound signs of infection (redness, hotness or discharge).
2. 6 weeks post radiation for wound dehiscence
3. 3 months post radiation for local swelling or recurrence
4. 6 months post radiation for local recurrence, joint stiffness or pathological fractures.
The patients with postoperative radiotherapy:
1. will be assessed 3 weeks post radiation regarding wound signs of infection (redness, hotness or discharge).
2. 6 weeks post radiation for wound dehiscence
3. 3 months post radiation for local swelling or recurrence
4. 6 months post radiation for local recurrence, joint stiffness or pathological fractures.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
surgical resection with safety margin
• The patients with preoperative radiotherapy:
1. will be assessed 3 weeks post radiation regarding wound signs of infection (redness, hotness or discharge).
2. 6 weeks post radiation for wound dehiscence
3. 3 months post radiation for local swelling or recurrence
4. 6 months post radiation for local recurrence, joint stiffness or pathological fractures.
The patients with postoperative radiotherapy:
1. will be assessed 3 weeks post radiation regarding wound signs of infection (redness, hotness or discharge).
2. 6 weeks post radiation for wound dehiscence
3. 3 months post radiation for local swelling or recurrence
4. 6 months post radiation for local recurrence, joint stiffness or pathological fractures.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Lesion: any soft tissue sarcoma in upper or lower limbs (synovial sarcoma, liposarcoma, fibrosarcoma and others)
* age more than 16 years old
Exclusion Criteria
* Round cell ESTS
* recurrent ESTS
* patients who received local irradiation due to other causes
16 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ain Shams University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ziad Khaled Abdullah Abdul Qader
orthopedic oncology department assistant lecturer
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ain Shams University Hospitals
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ziad khaled
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.