FindTrial
Sign In

Prevalence of Anxiety and Depression in patients undergoing surgery a day prior and 48 hours after surgery

PADon Study: Prevalence of Anxiety and Depression In Oncology Patients During Perioperative Period And Its Effect On Perioperative Pain Prospective,observational single center study. - PADOn

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/03/081518
Enrollment
336
Registered
2025-03-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: NA: NIL Control Intervention1: NA: NIL

Sponsors

Department of Anesthesia , Critical Care and Pain
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American society of Anesthesiologists (ASA) Grade I -III Patients undergoing oncological surgeries for:- Gynecological Procedures Orthopedic Procedures Gastrointestinal Procedures Urological Procedures Thoracic Procedures Head and Neck Procedures Requiring postoperative admission in the hospital ward for a minimum 48 hours

Exclusion criteria

Exclusion criteria: 1 Patients unwilling to participate in the study. 2 Difficulty in communication because of language limitation or planned tracheostomy in the postoperative period. 3 Patients already receiving psychoactive medications. 4 Surgeries with expected cognitive impairment in the post-operative(Any pre-existing cognitive defects or Neurosurgeries). 5 Patients previously diagnosed with major depressive disorder/other forms of depression and generalised anxiety disorder and may or may not be on treatment for the same. 6 Patients undergoing surgery for recurrent or second cancer. WITHDRAWAL CRITERIA: Patients needing ICU care for more than 48 hours,post operatively.

Design outcomes

Primary

MeasureTime frame
The prevalence of anxiety will be reported as proportions with 95% confidence intervals. Timepoint: One day before and 48 hours after surgery—

Secondary

MeasureTime frame
1. To study the prevalence of depression and to assess the severity of Anxiety and Depression in the postoperative period 2. To study the association between anxiety and depression and the perioperative Pain scores following oncological surgery using Numerical Rating Scale (NRS). 3. To assess the probable causes attributing to perioperative anxiety and depression in oncologic patients. 4. To assess the willingness of the postoperative patients to distraction or relaxation therapy and to correlate the same with their anxiety and depression scores. Timepoint: 48 hours after surgery—

Countries

India

Contacts

Public ContactDr Hemanshi

Tata Memorial Hospital

sumitrabakshi@yahoo.in02224177058

Outcome results

None listed

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