A Research study comparing pain relief effectiveness between Erector Spinae plane block and Quadratus Lumborum block in adult elective abdominal hysterectomy surgeries.

Comparision of analgesic efficacy between USG guided Erector Spinae Plane Block and Quadratus Lumborum Block in adult elective abdominal hysterectomy surgeries under Spinal Anaesthesia - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/068654

Enrollment

Registered

2024-06-11

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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: Erector Spinae Plane Block: The enrolled patients will be randomly allocated via computer generated random numbers into 2 groups and will be given 0.5% Levobupivacaine USG guided bilate

Eligibility

Inclusion criteria

Inclusion criteria: 1. BMI between 24-30 kg/m2 2. height between 150-170 cm 3. Duration of Surgery-1.5 to 2 hours 4. Patients of ASA 1 and 2 5. patients undergoing Total Abdominal Hysterectomy

Exclusion criteria

Exclusion criteria: 1.Patient refusal for procedure 2.Patients having Coagulopathy 3.Patients having cerebrovascular disease 4.Patients having systemic infection 5.Inability to understand the study protocol 6.Patients who have Allergy to local anesthetics 7.Psychopathy that may affect patient evaluation 8.Pregnant Patients 9.Infection at site of injection 10.Patients with Liver disease 11.Patients with kidney disease

Design outcomes

Primary

Measure	Time frame
1.To compare the duration of analgesia between Erector Spinae Plane Block and Quadratus Lumborum block . 2.To compare the total dose of tramadol needed as rescue analgesia in post operative 48 hours in both groups. Timepoint: 48 hours	—

Secondary

Measure	Time frame
1.To compare the hemodynamic parameters between the groups. 2.To compare any side effects between groups. Timepoint: 48 hours	—

Countries

India

Contacts

Public ContactDr Bhupendra Singh

All India Institute Of Medical Sciences, Raebareli

abhiraj997@gmail.com9694744962

Outcome results

None listed

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