Retained Products of Conception, Uterine Polyp
Conditions
Brief summary
Background: Small-diameter operative hysteroscopes may allow to perform operative hysteroscopy without general anesthesia in selected patients. One of these instruments is the tissue removal device (TRD), which resects and removes intrauterine pathology such as endometrial polyps and retained products of conception (RPOC) with a diameter of ¬6 mm. Objective: To assess the success rate and intraoperative pain of patients undergoing operative hysteroscopy without anesthesia with the TRD (TruClear Elite Mini-Hysteroscope) for removal of endometrial polyps or RPOC. Methods: Prospective observational study. Participation in the study was offered to patients diagnosed with uterine polyps or RPOC on office diagnostic hysteroscopy. The patients filled out a digital questionnaire before and after the operation. A successful procedure was defined as complete hysteroscopic removal of the uterine pathology using the TruClear system. Oral 400 mcg misoprostol 12 hours before the procedure was prescribed for cervical ripening.
Interventions
PROCEDUREhysteroscopy
Surgical hysteroscopy without anaesthesia for removal of uterine polyp / retained products of conception.
Sponsors
Assaf-Harofeh Medical Center
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Inclusion criteria
* Diagnosis of polyp or retained products of conception in diagnostic hysteroscopy. * Medical need to remove the finding according to accepted criteria. * Patient's consent to the removal of the finding in a procedure without anesthesia. * Patient's consent to participate in the study.
Exclusion criteria
* Any indication for performing the procedure under anesthesia in an operating room, such as: 1. Medical background requiring operation in an operating room. 2. Personal / mental background requiring procedure under general anesthesia. 3. Cervical stenosis 4. Previous failure to remove the finding in a procedure without anesthesia 5. Lack of response to performing the operation without anesthesia * The lack of response to participate in the study * A known diagnosis of malignancy from a previous sample of the polyp or endometrium
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Procedure completed successfully | Immediately after procedure | Was the procedure completed - yes/no |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Prevalence of VAS (pain scale) > 5 during procedure | Immediately after procedure | VAS (Visual analogue scale 0-10, most painful 10) grading by the patient |
| Prevalence of VAS (pain scale) > 5, five minutes after procedure | 5 minutes after procedure | VAS (Visual analogue scale 0-10, most painful 10) grading by the patient |
| Acceptable procedure by the patient | 5 minutes after procedure | Was the procedure acceptable by the patient (1-4 when 1 is most acceptable) |
| Recommended procedure by the patient | 5 minutes after procedure | Would the patient recommend her acquittance the procedure in this outline (1-5, most recommended 5) aquitance (1-5) |
Countries
Israel
Outcome results
None listed