Actively Recruiting
Reproductive Hormones During Sustained Administration of Kisspeptin
Led by Imperial College London · Updated on 2024-09-19
76
Participants Needed
1
Research Sites
712 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
We want to find out what happens to reproductive hormone levels; Luteinising Hormone (LH), Follicle Stimulating Hormone (FSH), testosterone and oestradiol when kisspeptin is administered to people for a period of 8 days each month, using either placebo (saline) or kisspeptin in doses of 0.1, 0.3 or 1.0 nmol/kg/hour.
CONDITIONS
Official Title
Reproductive Hormones During Sustained Administration of Kisspeptin
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18-60 years old
- Ability to give informed consent
- Secondary hypogonadism or healthy participant
You will not qualify if you...
- Anaemia
- Severe heart, kidney, or liver disease
- Blood donation within 3 months before or planned within 3 months after the study
- Needle phobia
- Poor venous access
- Active psychiatric illness
- Severe allergies
- Impaired ability to provide full consent
- Current alcohol or illicit drug dependence
- Current pregnancy or breastfeeding
- Plans to conceive within 3 months of starting the study (barrier contraception required during and 3 months after study)
- Arthritis or hand coordination problems preventing pump use
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Imperial College NHS Healthcare Trust
London, United Kingdom, W12 0NN
Actively Recruiting
Research Team
A
ALi Abbara, PhD MRCP
CONTACT
D
Debbie A Papadopoulou, BSc MRes
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
4
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