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Trial Title: Fecal Continence Outcomes and Quality of Life After Excision of Sacrococcygeal Teratoma (Retrospective Study)

NCT ID: NCT06133036

Condition: Sacrococcygeal Teratoma

Conditions: Official terms:
Teratoma

Study type: Observational

Overall status: Recruiting

Study design:

Time perspective: Retrospective

Summary: Sacrococcygeal teratoma is one of the most common tumors that occur in the neonatal period. It presents either as a mass protruding from the sacrococcygeal region or as a pelviabdominal mass according to the type. Surgical excision is the main treatment, most masses are benign, however some are malignant and require radiotherapy or chemotherapy. Complications may occur due to pressure resulting from the tumor growth in the fetal period, or due to damage to important near tissues during surgical excision. Postoperative complications may be urinary as neurogenic bladder, Lower gastrointestinal as constipation, soiling or incontinence. In this work we study the outcomes of fecal continence through a questionnaire and its effect on the quality of life of the affected children.

Criteria for eligibility:

Study pop:
Patients operated in Sohag university hospital after july 2010 for sacrococcygeal teratoma.

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - all patients with sacrococcygeal teratoma operated after july 2010 and older than 3 years old. Exclusion Criteria: - Patients lost to follow up before 6 months after surgery. - Patients with Currarino triad.

Gender: All

Minimum age: 3 Years

Maximum age: 18 Years

Healthy volunteers: No

Locations:

Facility:
Name: Sohag University Hospitals

Address:
City: Sohag
Zip: 82511
Country: Egypt

Status: Recruiting

Contact:
Last name: Mohamed K Khalil

Phone: +201028900808
Email: mohamedkamal@med.sohag.edu.eg

Start date: November 2023

Completion date: May 2024

Lead sponsor:
Agency: Sohag University
Agency class: Other

Source: Sohag University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06133036

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