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A study correlating the perioperative anxiety and depression in cancer patients with the dose of sedation required for introducing a breathing tube via a flexible scope

A prospective cohort study correlating the perioperative anxiety and depression in oncosurgical patients with the dose of sedation required for awake fibreoptic intubation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/03/050388
Enrollment
54
Registered
2023-03-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx

Interventions

None listed

Sponsors

Lokmanya Tilak Municipal Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Oncosurgical patients with planned awake intubation

Exclusion criteria

Exclusion criteria: 1) Patients with pre-existing psychiatric illness or on psychotropic medication. 2) Patients not willing to particiapte in study. 3) Pateints unable to understand Hindi, English , Marathi

Design outcomes

Primary

MeasureTime frame
The dosage of sedation required in oncosurgical patients undergoing AFOI depends upon their pre-operative anxiety and pre-existing depressionTimepoint: The sedation dose will be calculated immediately post induction ( 30 mins-1 hour)—

Secondary

MeasureTime frame
To calculate perioperative anxiety and depression using 3 scales namely- APAIS, MHADS and PHQ-9Timepoint: The scores will be administered at these time intervals PHQ-9 and MHADS- one day before APAIS - Pre-operatively( 1 hour before surgery)—

Countries

India

Contacts

Public ContactDr Aparna Nerurkar

Lokmanya Tilak Municipal Medical College

draparnanerurkar@gmail.com09833944243

Outcome results

None listed

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