Comparison of DuoFertility, LadyComp/BabyComp and Clearblue Monitors
NCT01364935 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2014-06-25
Summary
Comparative study to determine whether several fertility monitoring products - the DuoFertility monitor, the LadyComp/Babycomp monitor and Clearblue Ovulation tests - are substantially equivalent in performance, and secondarily to determine the appropriateness of labeling information for the DuoFertility monitor.
Conditions
Sponsors & Collaborators
-
Cambridge Temperature Concepts
collaborator INDUSTRY -
Cambridge University Hospitals NHS Foundation Trust
lead OTHER
Principal Investigators
-
Basil Matta · Cambridge University Hospitals NHS Foundation Trust
Eligibility
- Min Age
- 18 Years
- Max Age
- 44 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2011-03-31
- Primary Completion
- 2014-05-31
- Completion
- 2014-05-31
Countries
- United Kingdom
Study Locations
More Related Trials
-
Home Ovulation Test One Cycle at Home Study
NCT04667858 ·Status: COMPLETED
-
Digital Home Ovulation Test One Cycle at Home Study
NCT04667845 ·Status: COMPLETED
-
Clomifene Citrate as First Line Treatment in in Vitro Fertilization Cycles for Patients With Lower Ovarian Reserve
NCT01389713 ·Status: COMPLETED ·Phase: NA
-
Cumulative Live Birth After Double Stimulation Protocol Versus Antagonist Protocol for Poor Ovarian Responders
NCT05765968 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Does Clomiphene Citrate Used for Induction of Ovulation Effect Levels of AMH and Inhibin B
NCT02036411 ·Status: UNKNOWN
-
Cumulative Live Birth Rates in Dual Ovarian Stimulation Versus Two Antagonist Stimulations in Poor Ovarian Responders
NCT06093984 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Clinical and Live Birth Rates After Following Long Antagonist Protocol Versus Classical Antagonist Protocol
NCT03684421 ·Status: UNKNOWN
-
Study to Assess the Efficacy and Safety of Three Dosage Strengths of Pulsatile GnRH Delivered From a Iontophoretic Patch Compared to Oral Treatment With Clomiphene or Placebo in Infertile Females
NCT00796289 ·Status: COMPLETED ·Phase: PHASE2
-
Salivary Diagnostic Testing for IVF
NCT02040545 ·Status: COMPLETED
-
Clinical and Live Birth Rates After Following Long Antagonist Protocol Versus Long Agonist Protocol
NCT03693534 ·Status: UNKNOWN
-
Comparison of 2 Ovarian Stimulation Protocols for Women With Low Ovarian Reserve
NCT02128360 ·Status: UNKNOWN ·Phase: NA
-
AMH and Pregnancy Rate by Age During Stimulate In-Vitro Fertilization Protocol
NCT01762111 ·Status: WITHDRAWN
-
A Study to Compare the Safety and Efficacy of Cetrotide® 3 Milligram (mg) Versus Antagon™ in Women Undergoing Ovarian Stimulation
NCT00298025 ·Status: COMPLETED ·Phase: PHASE4
-
Clomiphene Citrate Plus Gonadotropins and GnRH Antagonist Versus Flexible GnRH Antagonist Protocol Versus Microdose GnRH Agonist Protocol in Poor Responders Undergoing IVF
NCT02201914 ·Status: UNKNOWN ·Phase: PHASE4
-
Evaluation of a Long Versus Short Clomid Protocol for Controlled Ovarian Stimulation
NCT06701071 ·Status: RECRUITING ·Phase: PHASE4
-
Mild Versus Conventional Ovarian Stimulation for Poor Responders Undergoing In Vitro Fertilisation
NCT01319708 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Post Market Surveillance & Post Market Clinical Follow up, International, Medical Registry to Confirm the Safety and the Performance of the Anecova Intra Uterine Culture Device
NCT03191890 ·Status: WITHDRAWN
-
Comparison of the Long GnRH Agonist Protocol and the Flexible GnRH Antagonist Protocol of Ovarian Stimulation
NCT00417183 ·Status: UNKNOWN ·Phase: PHASE4
-
Efficacy and Safety of Crinone Versus Combination Medication (ACCESS)
NCT03858049 ·Status: TERMINATED ·Phase: PHASE4
-
Progesterone Diurnal Rhythm During Ovarian Stimulation for IVF
NCT02975713 ·Status: TERMINATED
-
Use of Clomiphene Citrate as an Inhibitor of Ovulation in an Oocyte Cryopreservation Cycle
NCT05866068 ·Status: UNKNOWN
-
Comparison of Recombinant Follicle Stimulating Hormone and the Combination of Recombinant Follicle Stimulating Hormone With Clomiphene Citrate in Stimulated Intrauterine Insemination Cycles
NCT05670795 ·Status: RECRUITING ·Phase: NA
-
Norethindrone Impact on Receptiva Outcomes
NCT07134920 ·Status: COMPLETED
-
Combining LHu With Ultrasound Monitoring in IUI
NCT01205555 ·Status: TERMINATED ·Phase: NA
-
Patients Perspectives on Discontinuation of Their Fertility Treatment Due to the COVID-19 Pandemic
NCT04396210 ·Status: COMPLETED