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The Feasibility of Different Doses of Etomidate Admixed With Propofol in Induced Abortion: A Randomized, Double Blind Controlled Trial

T

Third Affiliated Hospital of Zhengzhou University

Status and phase

Unknown
Phase 4

Conditions

Induced Abortion
Anesthesia

Treatments

Drug: propofol
Drug: pentazocine
Drug: Etomidate

Study type

Interventional

Funder types

Other

Identifiers

NCT02208596
20140729

Details and patient eligibility

About

To explore the feasibility of different doses of etomidate admixed with propofol in induced abortion: a randomized, double blind controlled trial.

Enrollment

150 estimated patients

Sex

All

Ages

20 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged between 20 and 35 years
  • American Society of Anesthesiology (ASA) Physical Status: Ⅰ or Ⅱ
  • Singleton pregnancy and the gestational period is 6 to 8 weeks
  • Expected operation duration is within 60 minutes
  • The body weight should be within 15% around the standard weight
  • Signed informed consent form

Exclusion criteria

  • Serious cardiac, cerebral, liver, kidney, lung, endocrine disease
  • Upper respiratory infections within 4 weeks
  • Long use of hormone or history of adrenal suppression
  • History of use of glucocorticoids, aprotinin or immunosuppressant
  • Manifestation of immunodeficiency
  • History of use of sedatives or opiates
  • Needs of Neuromuscular blocker (except intubation)
  • Allergy to trial drug or other contraindication
  • Pregnant or breast-feeding women
  • Attended other trial past 30 days

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

150 participants in 3 patient groups

Group A
Experimental group
Description:
In group A, propofol (1%) was mixed with etomidate in the ration of 1:1 (volume). The mixture will be injected continuously until the eyelash reflex disappears. During the operation, supplementary mixture will be administered if the patient has spontaneous movement that hampered the conduct of the procedure.
Treatment:
Drug: propofol
Drug: Etomidate
Drug: pentazocine
Group B
Experimental group
Description:
In group B, propofol (1%) was mixed with etomidate in the ration of 7:5 (volume). The mixture will be injected continuously until the eyelash reflex disappears. During the operation, supplementary mixture will be administered if the patient has spontaneous movement that hampered the conduct of the procedure.
Treatment:
Drug: propofol
Drug: Etomidate
Drug: pentazocine
Group C
Experimental group
Description:
In group C, propofol (1%) will be injected continuously until the eyelash reflex disappears. During the operation, supplementary propofol will be administered if the patient has spontaneous movement that hampered the conduct of the procedure.
Treatment:
Drug: propofol
Drug: pentazocine

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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