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To study different pain modalities used in patients receiving Epidural analgesia for postoperative pain relief after elective Gynaecological Surgery

Dynamic Pain Scores in Patients Receiving Epidural Analgesia for Postoperative Pain Relief After Elective Gynaecological Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2016/04/006800
Enrollment
150
Registered
2016-04-05
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: null- Healthy patients (ASA physical status I and II), 18-60 years, scheduled to undergo elective gynaecological surgeries under combined spinal epidural anaesthesia will be included in the study.

Interventions

None listed

Sponsors

Lady Hardinge Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy patients (ASA physical status I and II), 18-60 years, scheduled to undergo elective gynaecological surgeries under combined spinal epidural anaesthesia will be included in the study

Exclusion criteria

Exclusion criteria: • ASA III and IV (Myocardial {NYHA class IIIâ??IV}, severe cerebrovascular, renal or hepatic impairment) • Refuse combined spinal epidural anaesthesia • Any contraindication to regional anaesthesia • History of drug allergy, contraindications to any of analgesic drugs, chronic use of opioids, non-steroidal anti-inflammatory drugs or corticosteroids • Inability to understand NRS or study protocol or unable to communicate • Patients in whom combined spinal epidural anaesthesia is inadequate for conduct of surgery will also be excluded from the study

Design outcomes

Primary

MeasureTime frame
To study dynamic pain scores which include pain on coughing and on movement from lying down to sitting position in patients receiving different epidural analgesia regimens for postoperative pain relief after elective gynaecological surgeryTimepoint: Patients will be observed at 1hr, 2hr, 4hr, 8hr and 12hr after surgery and at 8 am, 12 noon, 4pm and 8pm till epidural catheter is removed (48-96 hrs) after surgery.—

Secondary

MeasureTime frame
To study the difference in following parameters between different epidural analgesia regimens â?¢ Pain scores at rest. â?¢ Level of sensory blockade â?¢ Degree of motor blockade â?¢ Duration of analgesia after removal of catheter â?¢ Total analgesia requirement postoperatively â?¢ Side effects of drugs used â?¢ Difference in patient satisfaction scores â?¢ Catheter migration, if any Timepoint: Patients will be observed at 1hr, 2hr, 4hr, 8hr and 12hr after surgery and at 8 am, 12 noon, 4pm and 8pm till epidural catheter is removed (48-96 hrs) after surgery.—

Countries

India

Contacts

Public ContactDr Manpreet Singh

Lady Hardinge Medical College

ranjusingh1503@yahoo.com9811151285

Outcome results

None listed

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