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A Study on Methods Used to Control Pain After Laparoscopic Surgery

Effectiveness of various post operative pain management modalities among patients undergoing laproscopic surgeries an observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/103133
Enrollment
259
Registered
2026-02-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: Z488- Encounter for other specified postprocedural aftercare

Interventions

Intervention1: Nil: Nil

Sponsors

SRM Institute of Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 years and above. 2.Patients classified as American Society of Anesthesiologists (ASA) Physical Status I or II. 3.Patients willing to provide informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: Patients with ASA Physical Status III (i.e., ASA III, IV,) Patients with psychiatric or cognitive impairments affecting pain reporting. Patients with known hypersensitivity or allergy to any analgesic medications used in the study (e.g., opioids, NSAIDs, local anesthetics).

Design outcomes

Primary

MeasureTime frame
Patient satisfaction with postoperative pain management measured using the ASSIST - patient satisfaction survey (validated questionnaire).Timepoint: Patient satisfaction score assessed using the ASSIST patient satisfaction questionnaire, recorded once between 24 hours post operatively and the time of hospital discharge.

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactKumaragurudhasan

SRM Institute Of Science and Technology

karthikk1@srmist.edu.in9444586662

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026