WHO ICTRP trial
Duration of luteal support with progesterone pessaries to improve the success…
ISRCTN05696887 · International Standard Randomised Controlled Trial Number (ISRCTN) · Not Recruiting
Key facts
| Trial ID | ISRCTN05696887 |
|---|---|
| Public title | Duration of luteal support with progesterone pessaries to improve the success rates in assisted conception |
| Scientific title | Duration of Luteal Support with progesterone pessaries to improve the success rates in assisted conception: a randomised controlled trial |
| Primary sponsor | Liverpool Women's NHS Foundation Trust (UK) |
| Registry | International Standard Randomised Controlled Trial Number (ISRCTN) |
| Recruitment status | Not Recruiting |
| Study type | Interventional |
| Phase | Not Applicable |
| Countries | United Kingdom;England |
| Conditions | Infertilty Pregnancy and Childbirth Female infertility |
| Interventions | Patients will be randomised to two groups of treatments: Group A: Active drug. Cyclogest, Actavis UK PL00142/05/08. One pessary (400mg) vaginally or rectally twice daily for 8 weeks following positive pregnancy test. Group B: Placebo… |
| Registration date | Mar 26, 2012 |
| Target size | 460 |
| Secondary IDs | 2006-000599-33;EudraCT 2006-000599-33 |
| Registry page | isrctn.com |
At a glance
- No Results available
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: