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

Comparison of Bupivicain Alone With Bupivicain Plus Dexamethasone in Erector Spinae Plane Block For Post-Operative Analgesia After Thoracotomy

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05277974
Enrollment
30
Registered
2022-03-14
Start date
2022-02-15
Completion date
2022-07-10
Last updated
2022-03-14

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

Conditions

Post Operative Pain

Keywords

Erector Spinae Plane Block, Thoracotomy, Ultrasound

Brief summary

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.

Interventions

DRUGinj bupivicain

In goup B 30ml of inj. bupivicaine only will be given in Erector Spinae Plane Block and In Group D inj Bupivicain plus inj dexamethasone will be given

Sponsors

Sheikh Zayed Medical College
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
postoperative pain scores36 hours postoperativelyVisual Analogue Score is utilized to assess the postoperative pain

Countries

Pakistan

Contacts

Primary Contactamjad siddique, FCPS
dramjadsiddique74@gmail.com0689230165
Backup Contactsaira sadaf, FCPS
sairahbabar@live.com0689230165

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026