Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00909844
Other study ID # 2-54-52014-159
Secondary ID 2008-000565-39
Status Completed
Phase Phase 3
First received
Last updated
Start date April 2008
Est. completion date January 2016

Study information

Verified date January 2019
Source Ipsen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the protocol is to assess the efficacy of triptorelin 11.25 mg with respect to the proportion of children who maintain a regression or stabilisation of sexual maturity until the end of the study.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date January 2016
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- The child must have completed study 2-54-52014-143

- The child must have an effective response to 2 injections of triptorelin 11.25 mg according to investigator's evaluation with no significant treatment side effects

Exclusion Criteria:

- The patient has a known hypersensitivity to any of the test materials or related compounds

- The patient is unable or unwilling to comply fully with the protocol

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Triptorelin (I.N.N.)
Decapeptyl® SR 11.25mg

Locations

Country Name City State
France Hôpital Hôtel Dieu (CHU) Angers
France Medical Centre Bordeaux
France Hôpital Flaubert Le Havre
France Hôpital Archet II Nice
France Hôpital Robert Debré Paris
France American Memorial Hospital Reims
France Hôpital Charles Nicolle Rouen
France Hôpital Hautepierre Strasbourg
France Hôpital de la Gespe Tarbes
France Hôpital des Enfants Toulouse

Sponsors (1)

Lead Sponsor Collaborator
Ipsen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Children With a Stabilisation or Regression of Tanner Pubertal Stage at the End of the Study (Final Visit), Compared to Pretreatment (Month -6) and Baseline (Month 0) The primary objective was to assess efficacy of triptorelin pamoate 11.25 mg with respect to percentage of children maintaining a regression or stabilisation of sexual maturity (based on Tanner breast [girls] or genital [boys] pubertal stage) until end of study. Study treatment lasted until end of the therapeutic period; visits for Months 36 and 48 were optional since a child may have already finished the study at a prior visit. The Final Visit only occurred if the child did not end the study by a complete visit such as at Months 24, 36 or 48. Results are presented only for percentage of girls with regression or stabilisation of Tanner breast pubertal stage (n=34). Since only one boy was included in the study, results for this outcome measure were listed only and no statistical analysis was performed. Please also note additional post-hoc analysis for regression or stabilisation of Tanner breast pubertal stage which applied the variable Last Visit on Treatment instead of Final Visit. Months 12, 24, 36, 48 and Final Visit (if applicable; up to 63 months)
Secondary Percentage of Patients With a Suppressed Luteinizing Hormone (LH) Response to Gonadotropin-Releasing Hormone (GnRH) Test A suppressed LH response to the GnRH test was defined as a stimulated peak of LH =3 international units per litre (IU/L). Percentage of patients who had a suppressed LH response to the GnRH test is reported. It should be noted that almost no hormonal data was collected after Baseline; all data analysed is presented. Months -6, 0 and 36
Secondary Levels of Oestradiol in Girls or Testosterone in Boys Both Measured by Radioimmunoassay (RIA) Mean levels of oestradiol in girls or testosterone in boys are reported. It should be noted that almost no hormonal data was collected after Baseline; all data analysed is presented. Months -6, 0, 12, 36 and Final Visit (up to 63 months)
Secondary Percentage of Patients With a Suppressed Follicle Stimulating Hormone (FSH) Response to GnRH Test A suppressed FSH response to the GnRH test was defined as a stimulated peak of FSH =3 IU/L. Percentage of patients who had a suppressed FSH response to the GnRH test is reported. It should be noted that almost no hormonal data was collected after Baseline; all data analysed is presented. Months -6, 0 and 36
Secondary Body Mass Index (BMI) for Chronological Age Variation Mean changes of BMI from Pretreatment and from Baseline are reported. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Months -6, 0, 12, 24, 36, 48 and Final Visit (up to 63 months)
Secondary BMI Standard Deviation (SD) Score for Chronological Age Variation Mean changes of BMI SD score from Pretreatment and from Baseline are reported. SD score is a standard term used in growth studies and represents standard deviations calculated as the patient value minus the mean divided by the SD. SD scores vary depending on the age and sex of the child. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Months -6, 0, 12, 24, 36, 48 and Final Visit (up to 63 months)
Secondary Auxological Parameters Variations: Height SD Score Mean changes of height SD score from Pretreatment and from Baseline are reported. SD score is a standard term used in growth studies and represents standard deviations calculated as the patient value minus the mean divided by the SD. SD scores vary depending on the age and sex of the child. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Months -6, 0, 12, 24, 36, 48 and Final Visit (up to 63 months)
Secondary Auxological Parameters Variations: Growth Velocity SD Score Mean changes of growth velocity SD score from Pretreatment and from Baseline are reported. SD score is a standard term used in growth studies and represents standard deviations calculated as the patient value minus the mean divided by the SD. SD scores vary depending on the age and sex of the child. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Months -6, 0, 12, 24, 36, 48 and Final Visit (up to 63 months)
Secondary Auxological Parameters Variations: Weight Variation Mean changes of weight from Pretreatment and from Baseline are reported. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Months -6, 0, 12, 24, 36, 48 and Final Visit (up to 63 months)
Secondary Predicted Adult Height SD Score Mean change of predicted adult height SD score from Pretreatment and from Baseline are reported. SD score is a standard term used in growth studies and represents standard deviations calculated as the patient value minus the mean divided by the SD. SD scores vary depending on the age and sex of the child. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Also note that data for this endpoint was analysed for girls only. Months -6, 0, 12 and Final Visit (up to 63 months)
Secondary Bone Age Maturation Mean change in difference between bone age and chronological age from Pretreatment and from Baseline are reported. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Months -6, 0 and Final Visit (up to 63 months)
Secondary Percentage of Girls With a Uterine Length < 36 Millimetres (mm) Percentage of girls who had a uterine length < 36 mm are reported. It should be noted that only limited patient data was collected after Baseline; all data analysed is presented. Months -6, 0, 12, 24, 36 and Final Visit (up to 63 months)
Secondary Percentage of Children With a Stabilisation or Regression of Tanner Pubic Hair Pubertal Stage at the End of the Study (Final Visit), Compared to Pretreatment (Month -6) and Baseline (Month 0) Pubic hair was measured by the Tanner method on a scale of 1 to 6. A low grade (i.e. 1) corresponds to a pre-pubertal stage and a high grade (i.e. 5 or 6) to an adult stage. Percentage of patients who had stabilisation or regression (no change in grade or a reduced grade) of Tanner pubic hair pubertal stage is reported. Study treatment was to last until the end of the therapeutic period; visits for Months 36 and 48 were optional because if the girl was already 11 and the boy already 13, they would have finished the study at a prior visit. The Final Visit was to occur only if the child did not end the study by a complete visit such as at Months 24, 36 or 48. Please also note the additional post-hoc analysis for percentage of children with a stabilisation or regression of Tanner pubic hair pubertal stage which applied the variable Last Visit on Treatment instead of Final Visit. Months 12, 24, 36, 48 and Final Visit (if applicable; up to 63 months)
See also
  Status Clinical Trial Phase
Not yet recruiting NCT01944488 - LH Response to GnRH Test in Prepubescent Girls Under 6 Years N/A
Not yet recruiting NCT01944475 - Follow-up of Girls With Premature Thelarche and Precocious Puberty N/A
Completed NCT00564850 - Efficacy and Safety Study of Pamoate of Triptorelin in Children With Precocious Puberty Phase 3
Completed NCT00001181 - Testolactone for the Treatment of Girls With LHRH Resistant Precocious Puberty Phase 2
Recruiting NCT04113070 - Overweight and Obesity and Puberty Development Cohort Study
Recruiting NCT01601171 - Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate
Completed NCT00734279 - Follicle-Stimulating Hormone (FSH) and the Onset of Puberty Early Phase 1
Recruiting NCT05338411 - Effect of Exogenous Growth Hormone on Ocular Findings
Recruiting NCT06280807 - Observation of Environment and Reproductive-Endocrine Effects
Completed NCT00004344 - Purification of Testis-Stimulating Factor in Precocious Puberty N/A
Completed NCT00001202 - Treatment of Boys With Precocious Puberty Phase 2
Completed NCT04665713 - Effect of Prevalence of BMI on Efficacy of Herbal Medicines in Girls' Sexual Precocity
Completed NCT02199587 - The Effect of Medical Clown on the Pain and Anxiety Perception During LRH Analog Treatment or GH Provocation Test N/A
Terminated NCT04502836 - Evaluation of the Correlation Between Psychological Intervention, Including Providing Knowledge and Tools for Problems Solving, and the Anxiety Level of Female Patients Arriving to ACTH LRH Test - Pilot Study N/A
Completed NCT00006174 - Effects of Letrozole on Precocious Puberty Due to McCune Albright Syndrome Phase 1
Completed NCT02650141 - Clinical Trial of Experienced Chinese Herbal Formulas on Different Types of Precocious Puberty N/A
Completed NCT00004335 - Study of Gonadotropin-Releasing Hormone Pulse Frequency in Sexual Maturation and in the Menstrual Cycle N/A