Evaluate quality of recovery in trans oral robotic surgery
Not Applicable
- Conditions
- Health Condition 1: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynx
- Registration Number
- CTRI/2023/01/049140
- Lead Sponsor
- HCG Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients planned for trans-oral robotic oncosurgery, irrespective of chemo-immuno- hormonal-irradiation therapy received, willing to participate in the study.
Exclusion Criteria
1) Patients not willing to be a part of the study.
2) Patients with cognitive dysfunction, functional inability, debility and disability.
3) Emergency surgeries.
4) Conversion from minimally invasive robotic surgery to open surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of recovery scoreTimepoint: 1 hour postoperative period till 48 hours after surgery
- Secondary Outcome Measures
Name Time Method Patient satisfaction score <br/ ><br>Length of stay in intensive care unit and hospitalTimepoint: Post surgery till hospital discharge