Comparative study of general anesthesia and low dose spinal anesthesia in hysteroscopic patients on postoperative pain, nausea and vomiting

Comparative study of the effect of general anesthesia and low dose spinal anesthesia in hysteroscopy on postoperative pain, nausea and vomiting

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120201008897N9

Enrollment

Registered

2021-05-23

Start date

2021-04-21

Completion date

Unknown

Last updated

2021-05-26

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

Conditions

Candidates for hysteroscopy based on the opinion of a gynecologist.

Interventions

Intervention 1: Intervention group: People undergoing general hysteroscopy under general anesthesia. Intervention 2: Intervention group: People undergoing low-dose spinal hysteroscopy.

Eligibility

Sex/Gender

Female

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Candidate for hysteroscopy based on the opinion of a gynecologist In terms of anesthesia in II and I ASA Consent to enter the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain score based on Visual Analogue scale - nausea and vomiting. Timepoint: The first 15 minutes of recovery - when discharge - 4 hours after surgery. Method of measurement: Patient pain rate based on Visual analoguse scale - nausea and vomiting based on patient question (yes - no).	—

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsafoura rouholamin

Esfahan University of Medical Sciences

s_rouholamin@med.mui.ac.ir+98 31 3663 9903

Outcome results

None listed

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