Skip to content

Quality of Pain Relief Provided by Infiltration of Morphine Sulphate at the Surgical Wound in Patients Having Spine Fixation Surgery

“Analgesic Efficacy of Morphine Sulphate for Wound Infiltration in Patients Undergoing Spine Surgery: A Randomized Controlled Trial ?. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057553
Enrollment
70
Registered
2023-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intervention : Surgical site will be infiltrated with 20 ml of 0.25 mg/ml of morphine sulphate.: We aim to conduct a double blind randomized controlled trial containing two groups with

Sponsors

Sir Ganga Ram Hospital, New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with -Written informed consent -Gender: Males and Females -Age: 18 - 64 years -Physical Status: ASA grade I/II

Exclusion criteria

Exclusion criteria: Patients with -Known renal dysfunction -Known hepatic dysfunction -Known endocrinal disease -History of allergy/hypersensitivity to the drugs under study -History of substance abuse -Anticipated postoperative ventilation

Design outcomes

Primary

MeasureTime frame
Postoperative pain evaluation during first 72 hours as assessed by Numerical rating scale (NRS). Timepoint: 30min 60min 90min 2hrs 6hrs 12hrs 24hrs 48hrs 72hrs

Secondary

MeasureTime frame
-Requirement of first rescue analgesia in morphine sulphate & placebo (normal saline) groups from wound infiltration. -Supplemental analgesic requirement up to 72 hrs post-surgery in morphine sulphate & placebo groups after wound infiltration. -Assessment of side effects like sedation, nausea, & vomiting for 72 hrs post-surgery.Timepoint: ANALGESIC CONSUMPTION OF FENTANYL CITRATE VIA INTRAVENOUS PCA PUMP :at 1st dose then at 30 min 60 min 90 min 2 hrs 6 hrs 12 hrs 24 hrs 72 hrs DICLOFENAC SODIUM REQUIREMENT: 12-24hrs 24-48 hrs 48-72 hrs PONV (postoperative nausea & vomiting) will be assessed at 1 hr, 2 hrs, 6 hrs, 12 hrs, 24 hrs, 48 hrs & 72 hrs Richmond agitation sedation scale at 1 hr, 2 hrs, 6 hrs, 12 hrs, 24 hrs, 48 hrs & 72 hrs

Countries

India

Contacts

Public ContactShivam Sharma

Sir Gangaram hospital, New Delhi

bhuwancp@gmail.com9999200881

Outcome results

None listed

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