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Kisspeptin-10

KP-10, Metastin (45-54), Kisspeptin-10 (human), KiSS-1

Quick Stats
Studies 877
Trials 47
Completed PHASE2 INTERVENTIONAL NCT01667406

The Use of the Hormone Kisspeptin in 'in Vitro Fertilisation' (IVF) Treatment

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

We want to find out if kisspeptin is successful in stimulating oocyte maturation when it is used as a 'trigger' injection during IVF therapy for infertility.

Detailed Description

Participants in the study will have a standard Gonadotrophin Releasing Hormone (GnRH) antagonist IVF cycle, but instead of having a trigger injection of hCG (human chorionic gonadotrophin) they will be randomised to receive one of 4 doses of kisspeptin injection. Oocytes will be retrieved and graded by an embryologist to see whether or not they have matured. The reproductive hormones Luteinising hormone, follicle stimulating hormone, oestradiol and progesterone will also be measured

Interventions

Name: Kisspeptin 1.6nmol/kg
Type: DRUG
Description: single kisspeptin dose 1.6 nmol/kg subcutaneously
Name: Kisspeptin 3.2nmol/kg
Type: DRUG
Description: single kisspeptin dose 3.2 nmol/kg subcutaneously
Name: Kisspeptin 6.4nmol/kg
Type: DRUG
Description: single kisspeptin dose 6.4 nmol/kg subcutaneously
Name: Kisspeptin 9.6nmol/kg
Type: DRUG
Description: single kisspeptin dose 9.6 nmol/kg subcutaneously
Name: Kisspeptin 12.8nmol/kg
Type: DRUG
Description: single kisspeptin dose 12.8 nmol/kg subcutaneously
Name: Kisspeptin 9.6 nmol/kg double
Type: DRUG
Description: kisspeptin dose 9.6 nmol/kg given twice 10hrs apart subcutaneously
Name: Kisspeptin 9.6 nmol/kg + saline
Type: DRUG
Description: kisspeptin dose 9.6 nmol/kg subcutaneously and saline subcutaneously, 10hrs apart

Primary Outcomes

Measure: Percentage of Oocyte Maturation
TimeFrame: 36 hours post Kisspeptin-54 trigger injection
Description: This was assessed by oocyte yield (percentage of mature \[metaphase 2; M2\] oocytes collected from the number of follicles ≥ 14 mm on final ultrasound scan prior to kisspeptin-54 trigger administration

Trial Information

NCT ID

NCT01667406

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE2

Sponsor

Imperial College London

Last Updated

December 15, 2025