The Effects of Melatonin Treatment on Bone, Marrow, Sleep and Blood Pressure

Sponsor
University of Aarhus (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04864509
Collaborator
(none)
40
2
37

Study Details

Study Description

Brief Summary

Melatonin protects your bones while losing fat! This was previously demonstrated by our group. The mechanisms behind these findings are still elusive, and the aim of the present study is to assess the mechanisms.

In a double-blinded randomized controlled trial 40 postmenopausal woman are randomized to receive either 10 mg melatonin or placebo nightly for three months. Changes in gene expression in marrow cells will be assessed through micro array. Markers of bone metabolism will be assessed through biochemical markers. Cardiovascular health will be measured by tonometry and 24h blood pressure.

The results of the study will contribute with important knowledge about the beneficial effects of melatonin making it an interesting supplement to known treatment regimens against osteoporosis and overweight.

Condition or Disease Intervention/Treatment Phase
  • Drug: Melatonin 10 MG
  • Drug: Placebo
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
double blinded
Primary Purpose:
Treatment
Official Title:
The Effects of Melatonin Treatment on Bone, Marrow, Sleep and Blood Pressure in Post Menopausal Women
Anticipated Study Start Date :
May 1, 2021
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Melatonin 10mg

Nightly oral dose

Drug: Melatonin 10 MG
Nightly dose

Placebo Comparator: Placebo

nightly oral dose

Drug: Placebo
Nightly dose

Outcome Measures

Primary Outcome Measures

  1. Gene expression [After study completion. Up to one year]

    Changes in gene expression in human mesenchymal stem cells.The biopsies are put on freeze after obtaining them. All biopsies are analysed at once.

Secondary Outcome Measures

  1. Biochemical markers [After study completion. Up to one year]

    Changes in biochemical markers of bone metabolism measured in blood: Markers include PTH (pmol/l), ionized calcium (mmol/l) CTX (ug/l). Although different units they all contribute to the overall evaluation of bone metabolism and must therefore be regarded as the same outcome measure

  2. Quality of sleep [After study completion. Up to one year]

    Assessed through the questionnaire Pittsburgh quality of sleep questionnaire. A validated questionnaire assessing the quality of sleep. A score between 0-5 indicates a good quality of sleep. Scores above 5 indicate a poor quality of sleep.

  3. Cardiovascular health [After study completion. Up to one year]

    Changes in 24h blood pressure and arterial stiffness measured by standardized equipment

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years to 75 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Post-menopausal women between 55 and 75 years
Exclusion Criteria:
  • Severely impaired renal function

  • Severely impaired hepatic function

  • Coagulation factors PP<0.6

  • Hypercalcemia (p-ion calcium >1.32 nmol/l)

  • Previous or present malignancies (except a treated skin cancer that is not melanoma or treated carcinoma in situ, 2 years since last therapy)

  • Diseases affecting the calcium homeostasis including untreated thyroid diseases

  • Regular use of medicine affecting the calcium homeostasis, including diuretics, fenemal, lithium, antiepileptica and glucosteroids

  • Selective serotonin reuptake inhibitor (SSRI)-products with fluvoxamin

  • Treatment with carbamazepin

  • Treatment with rifampicin

  • Severe malabsorption syndrome including gastric or intestinal resection

  • Alcohol or drug abuse

  • Smokers

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Aarhus

Investigators

  • Principal Investigator: Anne Kristine Amstrup, Aarhus University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT04864509
Other Study ID Numbers:
  • 2020-AKA
First Posted:
Apr 29, 2021
Last Update Posted:
Apr 29, 2021
Last Verified:
Jun 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 29, 2021