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The Effects of Morphine on Desflurane Consumption and Recovery Time

B

Baskent University

Status and phase

Completed
Phase 4

Conditions

Abdominal Hysterectomy (& Wertheim)

Treatments

Drug: Morphine

Study type

Interventional

Funder types

Other

Identifiers

NCT02362022
14.09.2007/88-4

Details and patient eligibility

About

Combination of volatile and opioid agents are used to achieve unconsciousness, haemodynamic stability and analgesia for surgical prosedures. This prospective, randomized, double-blind, controlled study evaluates the effects of two different doses of morphine sulphate (0.1 mg/kg and 0.2 mg/kg), on desflurane consumption, recovery characteristics, postoperative analgesic requirements and side effects during total abdominal hysterectomy.

Enrollment

90 patients

Sex

Female

Ages

40 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • undergoing total abdominal hysterectomy with general anaesthesia

Exclusion criteria

  • renal dysfunction (cre>1.2), liver failure, cardiovascular, psychiatric, allergic and metabolic disorders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

90 participants in 3 patient groups, including a placebo group

Group Saline
Placebo Comparator group
Description:
Group Saline (Group S) received i.v saline 0.9 % in 10 ml volume (n=30)
Treatment:
Drug: Morphine
Group Morphine 1
Active Comparator group
Description:
Group Morphine 1 (Group M1) received i.v morphine 0.1 mg kg-1, in 10 ml volume (n=30)
Treatment:
Drug: Morphine
Group Morphine 2
Active Comparator group
Description:
Group Morphine 2 (Group M2) received i.v morphine 0.2 mg kg-1, in 10 ml volume (n=30)
Treatment:
Drug: Morphine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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