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A study to determine the effect of Intrathecal Morphine in patients on Patient Controlled Analgesia (PCA) Pump with morphine for Postoperative Pain Relief after elective Laparotomy.

A Randomised Controlled Trial to assess the efficacy of Intrathecal Morphine in patients on Patient Controlled Analgesia (PCA) Pump with morphine for Postoperative Pain Relief after elective Laparotomy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015183
Enrollment
22
Registered
2018-08-03
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K631- Perforation of intestine (nontraumatic)

Interventions

Intervention1: Morphine: Intrathecal 200mcg single dose Control Intervention1: MORPHINE: Intravenous,PCA 1mg bolus 10 minutes lockout interval

Sponsors

SRM MEDICAL COLLEGE HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective laparotomy. Patients assessed under ASA I & II

Exclusion criteria

Exclusion criteria: Patients who have contraindication for subarachnoid block. Patients who are unable to use a PCA pump. Patients with a history of drug abuse or allergy to the study drugs

Design outcomes

Primary

MeasureTime frame
To compare total morphine consumption, patient satisfaction and visual analog scale scores.Timepoint: 48 hours—

Secondary

MeasureTime frame
Comparison of related adverse reactions like nausea, pruritis, sedation, respiratory depressionTimepoint: 48 hours—

Countries

India

Contacts

Public ContactDr Anand K

SRM Medical College Hospital and Research Institute

dranandkuppusamy@gmail.com9092982288

Outcome results

None listed

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