Safety and Efficacy of Distending Media Infusion by Manual Syringe Method for Hysteroscopic Procedures

Far Eastern Memorial Hospital

Status: Completed

Conditions: Hysteroscopic Surgery

Study type: Observational

Funder types: Other

Identifiers

NCT02101827

103006-E

Details and patient eligibility

About

To evaluate the safety and efficacy of manual syringe-infusion method in hysteroscopic procedures.

Full description

In order to minimize the amount of distending media infused during hysteroscopic procedures, investigators used manual syringe method for delivering of distending media during hysteroscopic procedures from June 2010 to November 2013 in our institute. The aim of this study was to evaluate the safety and efficacy of manual syringe-infusion method in hysteroscopic procedures.

The medical records of all women who received hysteroscopic procedures by manual fluid-infusion method or convention pump fluid infusion method between June 2010 and November 2013 will be reviewed. In order to reveal the superiority/inferiority of clinical outcome of women receiving manual fluid infusion method, perioperative outcomes will be compared.

Enrollment: 200 estimated patients

Sex: Female

Ages: 20+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Of greater than twenty-year-old female patients suffering from abnormal uterine bleeding, suspected endometrial lesions, endometrial polyp, or submucous myoma.
• Patients had hysteroscopic procedures for either diagnostic or therapeutic purpose from June 2010 to November 2013 in Department of Obstetrics & Gynecology in Far Eastern Memorial Hospital.

Exclusion criteria

• Female patients of less than twenty years-old.

Trial design

200 participants in 1 patient group

Hysteroscopic surgery

Description:

Women who received hysteroscopic surgeries or examinations