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Comparing the duration of effect of Ropivacaine with Fentanyl and Ropivacaine with Dexmedetomidine for postoperative pain relief in lumbar spine surgery

THE EFFECT OF ULTRASOUND GUIDED ERECTOR SPINAE BLOCK USING ROPIVACAINE WITH FENTANYL, ROPIVACAINE WITH DEXMEDETOMIDINE ON POSTOPERATIVE PAIN AND OPIOID CONSUMPTION IN PATIENTS UNDERGOING LUMBAR SPINAL SURGERIES-A ONE YEAR RANDOMISED CLINICAL TRIAL. - Erector spinae block for lumbar spine surgeries

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058443
Enrollment
60
Registered
2023-10-09
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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: Ropivacine with Fentanyl: The targeted transverse process is identified and entered in-plane at a 30-40 degree angle towards the posterior surface of the targeted transverse process usi

Sponsors

Kathramoni Mahitha Rani
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective lumbar spinal surgeries under general anaesthesia. 2. ASA grades I & II. 3. Patients willing to give informed consent

Exclusion criteria

Exclusion criteria: 1. Patients receiving chronic analgesic therapy 2. Patients with history of opioid dependence 3. Patients with bleeding disorders 4. Patients on anticoagulative medication 5. Patients who refused to consent

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia of erector spinae block using ropivacaine with fentanyl and ropivacaine with dexmedetomidine .Timepoint: To identify the duration of analgesia of erector spinae block using ropivacaine with fentanyl and ropivacaine with dexmedetomidine Starting from end of surgery - VAS 0 till 24hrs (1 day) postoperatively VAS 24.

Secondary

MeasureTime frame
To evaluate the total 24 hour opioid consumption in both the groups.Timepoint: 1 to 24 hrs post surgery

Countries

India

Contacts

Public ContactDr Chaitanya Kamat

Jawaharlal nehru medical college,Belagavi,Karnataka.

mahithamudhiraj@gmail.com7306707024

Outcome results

None listed

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