NCT06831695Not yet recruiting
Comparison of Surgical Outcomes of Craniotomy and Craniectomy in Posterior Fossa Lesions
Comparison Between Surgical Outcomes of Craniotomy and Craniectomy Among Patients with Posterior Fossa Lesion
Source: ClinicalTrials.gov · Last updated 18 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The purpose of this randomized controlled trial is to compare the surgical outcomes of craniotomy and craniectomy among patients with posterior fossa lesions. The study aims to determine differences in post-operative complications, hospital stay duration, and patient recovery between the two surgical techniques.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 10 Feb 2025
- Start date
- 4 Mar 2025
- Primary completion date
- Mar 2026
- Lead sponsor
- University of Health Sciences Lahore
- Diseases
- Childhood cancers
- NCT number
- NCT06831695
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 4 Mar 2025 to the primary completion date, Mar 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous posterior fossa surgery
Other
- Brainstem hematoma
- Tumors involving the overlying dura or bone
Who the study is looking for
- Patients diagnosed with posterior fossa lesions
- Age range: 7-70 years
- Patients with cerebellar hematoma (traumatic or spontaneous)
Age in the registry: 7 years to 70 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.