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Changes in vital signs in two ways of anesthesia with midazolam- fentanyl and propofol- fentanyl in patients with infertility surgery

Comparison of hemodynamic changesbetween two methods of sedation with midazolam - fentanyl and propofol - fentanyl in patients undergoing ovarian puncture surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013092814802N1
Enrollment
56
Registered
2016-05-25
Start date
2015-04-04
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility. Other disorders of the genitourinary system

Interventions

Intervention 1: Intervention group 1: Patients in group A Will be sedate by propofol 1mg/kg, fentanyl 1 micrograms/kg while receiving oxygen and N2O 4lit/min via bag- mask ventilation. After secu
Treatment - Drugs
Intervention group 1: Patients in group A Will be sedate by propofol 1mg/kg, fentanyl 1 micrograms/kg while receiving oxygen and N2O 4lit/min via bag- mask ventilation. After securing the sedati
Intervention group 2: will be sedate by midazolam 0.05mg/kg, fentanyl 1 micrograms/kg while receiving oxygen and N2O 4lit/min via bag- mask ventilation. After securing the sedation, surgery will beg

Sponsors

vice-chancellor for research and technology of Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
21 Years to 39 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: infertile women between 21 -39 years; normal blood pressure; class I and II ASA; lack of sensitivity to propofol, undergoing puncture elective surgery. Exclusion criteria: unwillingness to participate in the study; puncture procedure took more than 10 minutes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Systolic and diastolic blood pressure. Timepoint: Before induction, then 3, 5 and 10 minutes after induction. Method of measurement: Portable analog pressure gauge.;Heart rate. Timepoint: Before induction, then 3, 5 and 10 minutes after induction. Method of measurement: monitoring.;Respiratory rate. Timepoint: Before induction, then 3, 5 and 10 minutes after induction. Method of measurement: Observation chest in a minute.;Saturation of oxygen. Timepoint: Before induction, then 3, 5 and 10 minutes after induction. Method of measurement: Pulse oximeter probe.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsara adarvishi

Ahvaz Jundishapor University of Medical Sciences

adarvishi.s@ajums.ac.ir+98 61 3377 7966

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026