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0.05 mg Versus 0.1 mg Spinal Morphine for Reducing Morphine Requirement After Vaginal Hysterectomy

M

Mahidol University

Status and phase

Unknown
Phase 4

Conditions

Pain

Treatments

Drug: Morphine

Study type

Interventional

Funder types

Other

Identifiers

NCT01080911
Si073/2010

Details and patient eligibility

About

This study aims to compare the effect of spinal morphine between the dose 0.05 mg and 0.1 mg on the amount of morphine during the first 24 hours postoperative.

Enrollment

72 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female ASA 1-3
  • Undergoing vaginal hysterectomy with/without anterior and posterior vaginoplasty
  • Can operate PCA device

Exclusion criteria

  • History of allergy to the study drugs
  • History of bleeding tendency
  • History of infection at the back
  • Patient refuse to have spinal anesthesia
  • History of CAD or CVD

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

72 participants in 2 patient groups

spinal morphine 0.05 mg
Experimental group
Description:
spinal morphine 0.05 mg plus 0.5% heavy marcaine 3.5 ml
Treatment:
Drug: Morphine
Drug: Morphine
spinal morphine 0.1 mg
Active Comparator group
Description:
spinal morphine 0.1 mg plus 0.5% heavy marcaine 3.5 ml
Treatment:
Drug: Morphine
Drug: Morphine

Trial contacts and locations

1

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Central trial contact

Sirilak Suksompong, MD

Data sourced from clinicaltrials.gov

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