Trials / Unknown
UnknownNCT04340778
Comparative Safety and Efficacy of Vaginal Dinoprostone Versus Lidocaine-prilocaine Cream in Copper IUD Insertion
Comparative Safety and Efficacy of Vaginal Dinoprostone Versus Lidocaine-prilocaine Cream in Copper IUD Insertion in Nulliparous Women: a Randomized Controlled Trial
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 210 (estimated)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Accepted
Summary
the aim of the present study is to Compare Safety and Efficacy of Vaginal dinoprostone Versus Lidocaine-prilocaine Cream in copper IUD Insertion in nulliparous women: a randomized controlled trial
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | vaginal dinoprostone | vaginal dinoprostone 3 mg will be given 3 hours before copper IUD insertion plus inert placebo cream will be applied on the cervix at the time of IUD insertion |
| DRUG | Lidocaine-prilocaine Cream | Lidocaine-prilocaine Cream will be applied on the cervix at the time of IUD insertion plus vaginal placebo tablet will be given 3 hours prior to IUD insertion |
| DRUG | placebo | inert placebo Cream will be applied on the cervix at the time of IUD insertion plus vaginal placebo tablet will be given 3 hours prior to IUD insertion |
Timeline
- Start date
- 2020-04-30
- Primary completion
- 2020-08-30
- Completion
- 2020-09-05
- First posted
- 2020-04-10
- Last updated
- 2020-04-10
Source: ClinicalTrials.gov record NCT04340778. Inclusion in this directory is not an endorsement.