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A study to evaluate patients opinion on separate consent taken for Anaesthesia (loss of feeling in all or part of the body with or without loss of consciousness) in patients undergoing major abdominal cancer surgeries

Patient Perspectives on a Separate Informed Consent for Anaesthesia – A Single-arm Prospective Cohort Analysis in Patients Undergoing Major Onco-surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/03/041452
Enrollment
500
Registered
2022-03-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C15-C26- Malignant neoplasms of digestive organs Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: None: NA Control Intervention1: None: NA

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing major onco-surgeries

Exclusion criteria

Exclusion criteria: 1. Patients who are unwilling to give consent for the study

Design outcomes

Primary

MeasureTime frame
Compliance of consent process to the standard recommendationsTimepoint: Within 3 days of postoperative period—

Secondary

MeasureTime frame
1. To assess the adequacy of the informed consent process from the patient perspective 2. Assessment of patient perception regarding the best time for administration of anaesthesia consent 3. Assessment of patient perception regarding the best method to explain risks associated with anaesthesia Timepoint: Within 3 days of postoperative period—

Countries

India

Contacts

Public ContactDr Pandurang Limbaji Awchar

Tata Memorial Centre

rambulkar@hotmail.com9821790448

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026