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TO COMPARE THE EASE OF PERFORMING COMBINED SPINAL EPIDURAL ANAESTHESIA BY PARAMEDIAN ROUTE BETWEEN ULTRASOUND GROUP AND SURFACE LANDMARK GROUP OF PATIENTS POSTED FOR LOWER LIMB ORTHOPEDIC SURGERY.

COMBINED SPINAL EPIDURAL ANESTHESIA VIA PARAMEDIAN APPROACH IN PATIENTS FOR LOWER LIMB ORTHOPEDIC SURGERY: A PROSPECTIVE RANDOMISED COMPARATIVE STUDY OF ULTRASOUND ASSISTED VERSUS CONVENTIONAL SURFACE LANDMARK TECHNIQUE. - CSE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/08/026959
Enrollment
100
Registered
2020-08-04
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: M849- Disorder of continuity of bone, unspecified

Interventions

Intervention1: PARAMEDIAN TECHNIQUE OF COMBINED SPINAL EPIDURAL ANAESTHESIA USING PREPROCEDURAL ULTRASOUND SACNING.: COMBINED EPIDURAL AND SPINAL ANAESTHESIA WILL BE GIVEN IN ONE ATTEMPT USING 18 G TU

Sponsors

ESI PGIMSR BASAIDARAPUR NEW DELHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients falling in ASA Grade I and II 2. Patients with indication for CSE. 3. Patients coming for orthopedic lower limb surgery.

Exclusion criteria

Exclusion criteria: 1. Patients having clinical features of raised Intra Cranial Pressure. 2. Deranged coagulation profile 3. Platelet count 4. Skin site infection 5. Patient refusal 6. Previous spinal sugery.

Design outcomes

Primary

MeasureTime frame
First attempt successful needle puncture through paramedian approach for CSE, between surface landmark guided group and ultrasound assisted group.Timepoint: 2 MINUTES

Secondary

MeasureTime frame
. 1 Epidural space depth 2. Total procedural time 3. Block-associated pain score 4. Complications if any Timepoint: 3MINUTES ,10 MINUTES,15 MINUTES

Countries

India

Contacts

Public ContactMOHD ANAS KHAN

ESI PGIMSR

madhugupta2602@gmail.com9873581030

Outcome results

None listed

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