A Real-World EvidenceStudy of Different Surgical Procedures for Rectal cancer
Not Applicable
- Conditions
- Health Condition 1: C20- Malignant neoplasm of rectum
- Registration Number
- CTRI/2023/03/050448
- Lead Sponsor
- Intuitive Surgical Pvt. Ltd. India
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Subject who was 18 years of age or older at the time of surgery
2. Subject who has undergone any of open, laparoscopic and robotic assisted rectal resection for non-metastatic rectal cancer (Stage I-IIIb).
The intent of the surgery should have been curative.
Exclusion Criteria
1. Subject who has undergone any of open, laparoscopic and robotic assisted rectal resection for rectal cancer with a palliative intent
2. Subject who has undergone any of open, laparoscopic and robotic assisted rectal resection for metastatic rectal cancer
3. Subject who has undergone an emergency procedure for primary
treatment of rectal cancer (ie, radical rectal resection)
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of this study is to retrospectively assess the perioperative outcomes through discharge and the short-term clinical outcomes from discharge to 90 days after open, laparoscopic or robotic-assisted rectal resections for rectal cancerTimepoint: From discharge to 90 days after surgery
- Secondary Outcome Measures
Name Time Method The secondary outcome of this study is to retrospectively assess the oncological outcomes, progression-free survival, and overall survival from postoperative day 91 and beyond up to 5 years after open, laparoscopic, or robotic-assisted rectal resections for rectal cancerTimepoint: From postoperative, day 91 and beyond, up to 5 years after surgery