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Comparison of Two Different Anesthesia Methods in IVF Procedure

A

Acibadem University

Status and phase

Completed
Phase 4

Conditions

Oocyte Retrieval

Treatments

Drug: propofol bolus
Drug: propofol infusion

Study type

Interventional

Funder types

Other

Identifiers

NCT05631925
SBilgen

Details and patient eligibility

About

In this study; during the oocyte retrieval procedure, it was aimed to compare two different general anesthesia methods, in which propofol was administered as infusion according to the patient's Bispectral index system (BIS) value or in bolus doses according to the patient's clinic.The hypothesis of the study; during the oocyte retrieval process, when propofol is administered as an infusion and accompanied by BIS monitoring, adequate anesthesia level will be achieved with less amount of bolus doses according to the clinical condition of the patient.

Full description

130 patients over the age of 18, ASA I-II, who underwent oocyte retrieval for IVF treatment were included in the study. The patients divided into two groups. In induction, 2mg/kg fentanyl, 40mg lidocaine and 2mg/kg propofol administered to all patients. Patients in group 1; propofol added in bolus doses of 0.5mg/kg. Doses determined according to the clinical condition of the patient. Patients in group 2; propofol administered as 10mg/kg/hour infusion. The infusion dose adjusted so that the Bispectral index (BIS) is in the range of 40-60.

Enrollment

130 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Over 18 years
  • ASA I-II
  • Patients who underwent oocyte retrieval for IVF treatment

Exclusion criteria

  1. The patient does not want to participate
  2. ASA > II patients
  3. Patients under 18 years of age
  4. Patients who are allergic to the drugs used
  5. Patients with mental illness
  6. Patients with alcohol or substance addiction

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

130 participants in 2 patient groups

Group bolus
Active Comparator group
Description:
Propofol will be administered in bolus doses of 0.5mg/kg. Doses will be determined according to the clinical condition of the patient.
Treatment:
Drug: propofol bolus
Group infusion
Active Comparator group
Description:
Propofol will be administered as 10mg/kg/hour infusion. The infusion dose will be adjusted so that the Bispectral index (BIS) is in the range of 40-60.
Treatment:
Drug: propofol infusion

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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