Efficacy of pre operative Bilateral Erector Spinae Plane Block for post operative pain relief following laparoscopic surgeries
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2023/02/049809
- Lead Sponsor
- Dr Ankitha J Hiremath
- Brief Summary
Pain in the post operative period is one of the major complaints which impedes
recovery of the patient from anaesthesia and surgery. The components of post
operative pain include- Somatic pain, Visceral pain, Referred pain.
Laparoscopic surgery is a minimally invasive surgery. Although minimally
invasive, the amount of pain the patient suffers from in the immediate post-operative
period is quite significant.
Techniques like Thoracic Epidural Analgesia (TEA), Thoracic paravertebral
block, Quadratus lumborum block, Rectus sheath block (RSB) have been previously
used for providing post-operative analgesia following Laparoscopic
Cholecystectomy. However, these techniques are associated with major
complications.
Erector Spinae Plane Block (ESPB) is a interfascial plane block. A feature
unique to Erector Spinae Plane Block is that no nerve or plexus needs to be
identified to administer the block. This block targets the space between Erector
Spinae Sheath and Transverse process of the vertebra. The local anaesthetic
injected spreads craniocaudally blocking multiple vertebral levels. The drug also
spreads anteriorly blocking the dorsal rami, ventral rami and also the rami
communicates.
In this background the research question of the present study is to
evaluate the efficacy of ultrasound guided bilateral erector spinae plane block
using bupivacaine for post operative analgesia following laparoscopic surgeries.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 20
- Patients posted for elective laparoscopic surgeries.
- Age 18 years and more 3.
- American society of Anaesthesiologists class I and II.
- Patietnts with history of known allergy to bupivacaine 2.
- Alcoholism, drug abuse, psycological or other emotional problems that are likely to invalidate the informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Plane Block(ESPB) with bupivacaine for post-operative analgesia in patients From the time of block till the time of request of the first dose of rescue analgesia by the patient(within 24 hours) To assess the efficacy of pre-emptive ultrasound guided bilateral Erector Spinae From the time of block till the time of request of the first dose of rescue analgesia by the patient(within 24 hours) undergoing laparoscopic surgeries From the time of block till the time of request of the first dose of rescue analgesia by the patient(within 24 hours)
- Secondary Outcome Measures
Name Time Method To see for the presence of post operative nausea and vomiting, time to ambulation(able to walk with or without support) and the total need of rescue
Trial Locations
- Locations (1)
DR. B R AMBEDKAR MEDICAL COLLEGE AND HOSPITAL
🇮🇳Bangalore, KARNATAKA, India
DR. B R AMBEDKAR MEDICAL COLLEGE AND HOSPITAL🇮🇳Bangalore, KARNATAKA, IndiaDR ANKITHA J HIREMATHPrincipal investigator9980741849anku3025@gmail.com