MedPath

Effects of low thoracic erector spinal plane block for patients undergoing abdominal hysterectomy under general anaesthesia

Not Applicable
Completed
Conditions
Health Condition 1: N72- Inflammatory disease of cervix uteriHealth Condition 2: O- Medical and Surgical
Registration Number
CTRI/2021/04/032896
Lead Sponsor
JLN medical college Ajmer
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

Age group between 25 and 60 years

Body weight 30 to 80 kg

Patients belonging to ASA (American Society of Anaesthesiologists) class 1 and 2

Patients undergoing abdominal hysterectomy of duration 1 to 2 hours in theatre with haemoglobin atleast 9 gm/dl

Patient free from any associated acute or chronic systemic illness

Exclusion Criteria

Patients not willing to participate in the study

Uncooperative patients

Patient with chronic pain or on long-term analgesics

Any known hypersensitivity or contraindication to bupivacaine

Local pathology at the site of injection or disability limiting the performance of block,(deformity of spine)

Patients receiving beta blockers or cardiac drugs.

History of convulsion, allergy to the drug used, bleeding disorder, severe neurological deficit, thyroid disorder

Patient with history of respiratory, cardiac, hepatic or renal disease (necessitating classification in ASA Class III or above)

Patients having a history of significant neurological, psychiatric, or neuromuscular disorders

Pregnant, lactating mothers

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of Number and frequency of postoperative analgesia required in both the groups for First 36 hours Postoperatively <br/ ><br> To assess the effective analgesia by visual analog scale (VAS) scoreTimepoint: Around 1 year
Secondary Outcome Measures
NameTimeMethod
To assess and compare the hemodynamic changes . <br/ ><br>To assess and compare the proportion of patients having adverse effects and any �  other complications. �  �  �  �  �  � �  <br/ ><br>To assess Sensory and motor block if any in the ESPB group.Timepoint: Around 1 year
© Copyright 2025. All Rights Reserved by MedPath