drugset / Trial / NCT02539199
Vaginally Administered Versus Per Oral Misoprostol in Induction of Labour
Phase 4
Completed
270 enrolled
Tampere University Hospital
Helsinki University Central Hospital · collabOulu University Hospital · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to investigate the effectiveness and safety of vaginally administered misoprostol (Misodel) versus per orally administered misoprostol (Cytotec) in induction of labour in nulliparous women.
Timeline
- Start
- 2015-09
- Primary completion
- 2018-03-02
- Completion
- 2018-03-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Misoprostol | Other / unclassified | 7 ug | Other |
| Comparator | Misoprostol | Other / unclassified | 50 ug | Other |
| Comparator | Misoprostol | Other / unclassified | 100 ug | Other |
Indications
No indication recorded.