IUD Insertion Pain Clinical Trial
Official title:
the Effect of Vaginal Isosorbide Mononitrate Administration in Reducing Pain During Cooper Intrauterine Device Insertion in Nulliparous Women : a Randomized Controlled Trial
| Verified date | January 2021 |
| Source | Cairo University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aim of the study is to evaluate the efficacy of isosorbide mononitrate vaginal administration in reducing pain during copper IUD insertion in nulliparous women
| Status | Completed |
| Enrollment | 110 |
| Est. completion date | November 30, 2020 |
| Est. primary completion date | October 25, 2020 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | N/A and older |
| Eligibility | Inclusion Criteria: - nulliparous women requesting copper IUD device insertion Exclusion Criteria: - parous women, contraindications to IUD insertion, allergy or contraindication to isosorbide mononitrate, uterine anomaly |
| Country | Name | City | State |
|---|---|---|---|
| Egypt | Ahmed Samy | Giza |
| Lead Sponsor | Collaborator |
|---|---|
| Cairo University |
Egypt,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | pain during IUD insertion | intensity of patient-perceived pain at time of IUD insertion, using a visual analog scale. The VAS scale is graded from 0 to 100 on a 100 mm horizontal straight line, where 'zero' corresponds to no pain at all, and '100' to the worst possible pain imaginable. | 5 minutes | |
| Secondary | duration of IUD insertion | duration of IUD insertion from speculum in to speculum out | 5 minutes |
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