Study of Axillary Skin Temperature as a Marker of Ovulation
NCT ID: NCT01360684
Last Updated: 2018-06-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
10 participants
OBSERVATIONAL
2010-07-31
2015-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The DuoFertility sensor a CE marked Class la device provides a continuous accurate measure of axilla temperature whilst worn under the arm.
The investigators plan to compare the temperature measurements of the DuoFertility sensor with the gold standard transvaginal ultrasound scan obtained during 10 infertile women's menstrual cycles, up to 10 cycles per women.
The investigators aim to investigate if continuous axillary skin temperature measurement obtained from the DuoFertility sensor, provides comparable results for identifying the occurrence of ovulation as the gold standard transvaginal ultrasound scan.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Measuring Core Body Temperature Using TempuRing
NCT02462278
Continuous Temperature Measurement by Thermal Imaging Camera
NCT06256978
Principles and Test Methods of Non-contact Body Thermometry
NCT05247736
Handheld Infrared Thermometer to Evaluate Cellulitis
NCT03846635
Temperature Measurement in Post-Anesthesia Care Units
NCT00614588
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Females aged 18 to 44 years.
* Referred with infertility to the Reproductive Medicine Clinic, Rosie Hospital
* Have a body mass index (BMI) above 19 and below 29
* Regular menstrual cycles, i.e. no greater than 7 days difference between the shortest and longest cycle in the last 6 months
* Minimum menstrual cycle 21 days
* Maximum menstrual cycle 35 days
* Willing to wear a DuoFertility sensor continuously for 8 to 10 menstrual cycles;
* Willing to attend Rosie Hospital up to 5 times per cycle for TVS and blood tests
* Willing to perform twice daily LH urine tests at home from day 8 of cycle till positive
* Normal pelvic ultrasound and blood results obtained during screening tests
Exclusion Criteria
* Have a BMI less than 18 or greater than 29
* Any diagnosed systemic illnesses, including but not restricted to thyroid disease, diabetes or inflammatory diseases
* Polycystic ovary disease
* Endometriosis or other pelvic pathology (including proven tubal disease)
* Taking steroids, including oral contraceptives or anti inflammatory drugs
18 Years
44 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cambridge Temperature Concepts
INDUSTRY
Joanne Outtrim
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Joanne Outtrim
Senior Research Nurse
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Raj Mathur
Role: PRINCIPAL_INVESTIGATOR
Cambridge University Hospital NHS Foundation Trust
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Cambridge University Hospital NHS Foundation Trust
Cambridge, Cambridgeshire, United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
10/H0308/35
Identifier Type: OTHER
Identifier Source: secondary_id
A091932
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.