Post operative image guided pain relief with local anaesthesia in patients undergoing open nephrectomy

Ultrasound guided Erector Spinae Plane Block for post operative analgesia in patients undergoing open nephrectomy

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/09/027996

Enrollment

Registered

2020-09-23

Start date

Unknown

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

Health Condition 1: N288- Other specified disorders of kidney and ureter

Interventions

Intervention1: Ultrasound guided Erector Spinae Plane Block with general anaesthesia and PCA morphine in PACU: Patients will be given general anaesthesia and after surgery, before reversal of anaesthe

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA physical status I and II 2. Age between 18 to 60 years. 3. Scheduled for open nephrectomy surgery.

Exclusion criteria

Exclusion criteria: 1. Patient refusal for procedure. 2. Allergic to local anaesthetics. 3. Infection at local site. 4. Bleeding disorders. 5. Severe kidney dysfunction. 6. BMI above 30kg/m2. 7. Inabilty to give informed consent.

Design outcomes

Primary

Measure	Time frame
To study the total opioid consumption over 24 hours after erector spinae block following open nephrectomyTimepoint: To study the total opioid consumption over 24 hours after erector spinae block following open nephrectomy	—

Secondary

Measure	Time frame
To study any opioid related side effectsTimepoint: Any side effects from opiods within the first 24 hours.;To study patient satisfaction using a Likert- scale questionnaireTimepoint: Patient satisfaction about the overall pain management and quality of sleep at night on post operative day 0 using a Likert-scale with 0-6 score points;To study the pain intensity using Numeric Rating ScleTimepoint: Pain intensity using a 10 point Numeric Rating Scale at 30 minutes, 2,4,6,8,12,18,24 hours respectively.;To study the time of first analgesic used over 24 hoursTimepoint: Time for first requested analgesic from time in PACU till discharge.	—

Measure

Time frame

To study any opioid related side effectsTimepoint: Any side effects from opiods within the first 24 hours.;To study patient satisfaction using a Likert- scale questionnaireTimepoint: Patient satisfaction about the overall pain management and quality of sleep at night on post operative day 0 using a Likert-scale with 0-6 score points;To study the pain intensity using Numeric Rating ScleTimepoint: Pain intensity using a 10 point Numeric Rating Scale at 30 minutes, 2,4,6,8,12,18,24 hours respectively.;To study the time of first analgesic used over 24 hoursTimepoint: Time for first requested analgesic from time in PACU till discharge.

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Countries

India

Contacts

Public ContactDr Deepak Oberoi

Himalayan Institute of Medical Sciences

soumya.bindra@gmail.com9205208488

Outcome results

None listed

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