A Study Of Postoperative Pain Relief in Lumbar Spine Surgery Patients

A Comparative Study Of Bupivacaine Alone And Bupivacaine with Dexmedetomidine In Erector Spinae Plane Block For Postoperative Analgesia In Posterior Lumbar Spine Surgery - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/103604

Enrollment

100

Registered

2026-02-11

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: M472- Other spondylosis with radiculopathy

Interventions

Intervention1: Inj.Bupivacaine(0.25%)19 ml+inj. Dexmedetomidine (0.5mcg/kg): Inj.Bupivacaine(0.25%)19 ml+inj.Dexmedetomidine (0.5mcg/kg) will be given under USG machine guindance for ESP block in Pati

Eligibility

Inclusion criteria

Inclusion criteria: 1.Informed written consent 2.ASA Grade 1 to 3 3.Elective 1 or 2 level posterior Lumbar Spine Surgery under general anesthesia

Exclusion criteria

Exclusion criteria: 1.Patient refusing for consent 2.Infection at site of needle insertion 3.Coagulopathies 4.Known sensitivity or allergy to the study drugs

Design outcomes

Primary

Measure	Time frame
Pulse Systolic Blood Pressure Diastolic Blood Pressure Spo2Timepoint: vitals will be observed intra op(Base line,After induction, After Prone Position, At block After block at 10 min,30 min 60 min,80 min,120 min,180 min) And Post operatively(1hr,2hr,4hr,8hr,12hr,24hr)	—

Secondary

Measure	Time frame
Postoperative pain intensity using Numerical Rating Scale(NRS)Timepoint: 1 hour 2 hour 4 hour 8 hour 12 hour 24 hour	—

Countries

India

Contacts

Public ContactDhara Ram

GCS Medical College Hospital Research Centre Ahmadabad

drdeepa0202@gmail.com7874145408

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026