Postoperative pain relief in spine surgeries

Evaluation of Caudal Epidural Analgesia with 0.125% Bupivacaine for Postoperative Pain Relief in Adults undergoing Lumbosacral Spine Surgeries

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/03/032401

Enrollment

Registered

2021-03-30

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: O- Medical and Surgical

Interventions

Intervention1: Inj Bupivacaine 0.125% 20 ml: We will identify both sacral cornu and Under C arm Guidance we will pass 23 guage quinke spinal needle .Location of tip of needle confirmed with swoosh tes

Eligibility

Inclusion criteria

Inclusion criteria: patients undergoing surgeries for discetomy,laminectomy,laminotomy and spine fixation in lumbosacral spine by posterior approach.

Exclusion criteria

Exclusion criteria: Non consenting patient,Local site infection, Allergic to local anesthetic agents,Congenital spine anamolies

Design outcomes

Primary

Measure	Time frame
post operative pain quantified by Visual Analog ScaleTimepoint: immediate post operative,4 hours,8 hour,16 hours and 24 hours	—

Secondary

Measure	Time frame
any postoperative complications associated with local anesthesiaTimepoint: upto 24 hours	—

Countries

India

Contacts

Public ContactR Santhosh Kumar Gupta

Prathima Institute of Medical Sciences

santhoshkumargupta@gmail.com9440910035

Outcome results

None listed

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