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COMPARISON OF MEAN DURATION OF POST OPERATIVE ANALGESIA FOLLOWING ADDITION OF DEXMEDETOMIDINE TO ROPIVACAINE VERSUS PLAIN ROPIVACAINE ON ULTRASOUND GUIDED RECTUS SHEATH BLOCK

Q

Quaid-e-Azam Medical College

Status

Completed

Conditions

Midline Laparotomy

Treatments

Procedure: Rectus Sheath Block

Study type

Interventional

Funder types

Other

Identifiers

NCT07254130
BVH-2025-CT-012

Details and patient eligibility

About

To compare the mean duration of postoperative analgesia following addition of dexmedetomidine to ropivacaine versus plain ropivacaine in ultrasound guided rectus sheath block in patients undergoing midline laparotomies

Enrollment

209 patients

Sex

All

Ages

30 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with age 30 - 60 years.

  • Patients that will be scheduled for laparotomy under general anesthesia.
  • ASA (American Society of Anesthesiologist) s

Exclusion criteria

  • Patient who will refuse for participation in study.
  • Infection at site of Rectus Sheath block.
  • History of any addiction.
  • Sensitivity to the local anesthetics.
  • Patient with pre-existing coagulation abnormalities INR more than 1.5.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

209 participants in 2 patient groups

Ropivacaine only group
Active Comparator group
Treatment:
Procedure: Rectus Sheath Block
Dexmedetomedine combined with ropivacaine group
Active Comparator group
Treatment:
Procedure: Rectus Sheath Block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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