Effects of Propofol or sodium thiopental on treatment outcomes in patients undergoing reproductive assisted technologies

Propofol or sodium thiopental in patients undergoing reproductive assisted technologies: comparative efficacy in hemodynamic recovery from anesthesia and outcome of oocyte retrieval

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201303135393N2

Enrollment

Registered

2013-05-14

Start date

2012-04-27

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

Female infertility. Female infertility associated with male factors

Interventions

Intervention 1: propofol. Intervention 2: sodium thiopental.

Treatment - Drugs

propofol

sodium thiopental

Eligibility

Sex/Gender

Female

Age

20 Years to 35 Years

Inclusion criteria

Inclusion criteria: (inclusion criteria: lack of infertility problems in the women and the presence of fertility problems in their husbands; Informed consent) (Exclusion criteria: History of Hypertension; chronic respiratory diseases; thyroid disorders; severe side effects of drugs during the experiment)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Systolic blood pressure. Timepoint: 5, 10, 15, 20 minutes after sedation. Method of measurement: mmHg.;Diastolic blood pressure. Timepoint: before sedation. Method of measurement: mmHg.;Heart rate. Timepoint: before sedation. Method of measurement: mmHg.;Respiratory rate. Timepoint: before sedation. Method of measurement: counting.;Rapid response to vocal stimulant. Timepoint: 5, 10, 15 and 20 minutes after anesthesia. Method of measurement: observation.;Vommiting. Timepoint: After Anesthesia. Method of measurement: Observation.	—

Measure

Time frame

Systolic blood pressure. Timepoint: 5, 10, 15, 20 minutes after sedation. Method of measurement: mmHg.;Diastolic blood pressure. Timepoint: before sedation. Method of measurement: mmHg.;Heart rate. Timepoint: before sedation. Method of measurement: mmHg.;Respiratory rate. Timepoint: before sedation. Method of measurement: counting.;Rapid response to vocal stimulant. Timepoint: 5, 10, 15 and 20 minutes after anesthesia. Method of measurement: observation.;Vommiting. Timepoint: After Anesthesia. Method of measurement: Observation.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Dehghan Tezerjani

Shahid Sadoughi University of medical sciences

Drdehghan@gmail.com+98 35 1822 4000

Outcome results

None listed

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