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Comparison of three anesthesia methods in hysteroscopic surgery

Comparative evaluation of effect of General anesthesia, Spinal anesthesia and Paracervical block on pain, nausea, vomiting and analgesic requirements in diagnostic Hysteroscopy.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120915010841N26
Enrollment
66
Registered
2021-11-07
Start date
2021-12-05
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Hysteroscopic surgery under general anesthesia, spinal anesthesia or para cervical block.

Interventions

Intervention 1: Intervention group1: In all patients after entering the operating room, using a 18 intravenous lines, after receiving 5 ml/kg of serum Ringer, in general anesthesia group, 0.02mg/kg mi

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patients 18 to 45 years ASA class1&2 Candidate for diagnostic hysteroscopic surgery Satisfaction to participate in the study Do not use analgesics for 24 hours before surgery Absence of contraindications to spinal anesthesia and general anesthesia

Exclusion criteria

Exclusion criteria: History of allergies to local anesthetics and propofol Cardiac,respiratory,renal and liver diseases Candidate patients for myomectomy or polypectomy with resectoscope Electrolyte disturbances (sodium, potassium and calcium Uterine prolapse History of previous cervical or hysteroscopic surgery History of nausea and vomiting following previous anesthesia or history of motion sickness Lack of patient cooperation after initial interventions Coagulation disorders

Design outcomes

Primary

MeasureTime frame
Post operative pain. Timepoint: After surgery in recovery. Method of measurement: Using visual analog scale (VAS).;Analgesic requirement. Timepoint: After surgery in recovery. Method of measurement: Based on the amount of analgesia requested by the patient.

Secondary

MeasureTime frame
Systolic and Diastolic Blood Pressure. Timepoint: Before and after general or regional anesthesia, insertion of Spacolom and Tenacolom, dilation of cervix,insertion of hysteroscope, biopsy and extraction of hysteroscope. Method of measurement: Non-invasive automatic barometric device.;Nausea & vomiting. Timepoint: After surgery in recovery. Method of measurement: Observation.;Heart Rate. Timepoint: Before and after general or regional anesthesia, insertion of Spacolom and Tenacolom, dilation of cervix,insertion of hysteroscope, biopsy and extraction of hysteroscope. Method of measurement: Pulseoximetry.;Shivering. Timepoint: After surgery in recovery. Method of measurement: Observation.;Satisfaction rate. Timepoint: Before discharge from recovery. Method of measurement: Asking the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Manouchehrian

Hamedan University of Medical Sciences

manuchehriann@gmail.com+98 81 3827 7012

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 9, 2026