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Bupivicain vs Bupivicain Plus Dexamethasone in ESP Block for Post-op Analgesia

S

Sheikh Zayed Medical College

Status and phase

Unknown
Phase 3

Conditions

Post Operative Pain

Treatments

Drug: inj bupivicain

Study type

Interventional

Funder types

Other

Identifiers

NCT05277974
ASIDDIQUE SZMC

Details and patient eligibility

About

Thoracotomy is a very painful procedure. Different treatment modalities are being utilized for post-thoracotomy analgesia including I/V NSAID, Opoids and Neuropathic medications. Other techniques commonly utilized include Thoracic epidural, Paravertebral block; but both are associated with significant failure rate and other complications. Ultrasound guided Erector Spinae Plane block is a new regional anesthesia technique that provides analgesia at multidermatomal levels acriss the posterior, lateral and anterior thoracic walls. The rational of my study is that it is a novel technique and studies with bupivicain alone are present but no study was found with bupivicain plus dexamethasone.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age 18-60years ASA I-III Patients undergoing elective thoracotomies

Exclusion criteria

  • Refusal of Patient Coagulation disorders Known Allergy to Local Anesthetics Infection at the site of injection Pregnant females Morbid Obesity(BMI>40kg/m2) Psychiatric illness Diabetic Patients.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Group B.
Active Comparator group
Description:
group B will receive Inj Bupivicain only in Erector Spinae Plane Block.
Treatment:
Drug: inj bupivicain
Group D
Active Comparator group
Description:
group D will receive Inj Bupivicain plus Dexamethasone in Erector Spinae Plane Block.
Treatment:
Drug: inj bupivicain

Trial contacts and locations

2

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Central trial contact

amjad siddique, FCPS; saira sadaf, FCPS

Data sourced from clinicaltrials.gov

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