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Not Yet RecruitingNCT06959745

Magnesium-L-Threonate Improves Menopausal Symptoms

Magnesium-L-Threonate Improves Menopausal Symptoms: A Single-center, Single-blind, Randomized, Placebo-Controlled Pilot Study

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Guangdong Provincial People's Hospital · Academic / Other
Sex
Female
Age
40 Years – 60 Years
Healthy volunteers
Accepted

Summary

This trial has a randomized, single-blind, single-center, parallel-controlled design, with participant screening and trial implementation conducted at Guangdong Provincial People's Hospital. The study evaluate the efficacy of oral magnesium L-threonate supplementation on improving menopausal symptoms and quality of life among peri/post-menopausal women. This trial aims to explore whether oral magnesium L-threonate supplementation could alleviate menopausal syndromes. Participants will randomly assigned to conduct oral magnesium L-threonate supplementation or placebo for 8 weeks. Face-to-face and internet follow up will be conducted once per 2 weeks.

Detailed description

The peri-menopausal period is a crucial transitional stage for women from middle age to old age. During this period, there is a dramatic and continuous decline in estrogen levels in women's bodies. The rapid change in estrogen levels triggers a series of complex physiological and pathological changes, leading to many clinical symptoms in perimenopausal women. The menopausal syndrome encompasses osteoporosis and joint-muscle pain, hot flashes and night sweats in terms of vasomotor symptoms, mood swings and memory loss, etc. It greatly troubles women physically and mentally and affects their daily lives. Currently, the main treatment methods for menopausal syndrome include hormone replacement therapy (HRT) and selective serotonin reuptake inhibitors (SSRI). However, both of these treatment methods are accompanied by significant side effects. Hormone replacement therapy may increase the risk of diseases such as breast cancer, endometrial cancer, and venous thrombosis. Therefore, there is an urgent need to explore safe and effective new therapies to improve the health of perimenopausal women. Magnesium ions, as important cations in the human body, play an indispensable role in maintaining the normal physiological functions of the body. In perimenopausal women, due to the decrease in estrogen levels, the level of magnesium is greatly decreased. Magnesium deficiency not only aggravates the symptoms of menopausal syndrome but also may increase the risk of chronic diseases such as cardiovascular diseases and osteoporosis. However, traditional magnesium supplements, such as magnesium sulfate and magnesium oxide, have obvious limitations in practical applications. After oral administration, traditional magnesium supplements cannot effectively increase the intracellular magnesium concentration, and cannot cross the blood-brain barrier and are difficult to act on the nervous system to improve pain, hot flashes, and other menopausal symptoms. Magnesium L - threonate is a new magnesium supplement with unique advantages. It is an oral preparation that can effectively supplement intracellular magnesium. Its greatest feature is that it can smoothly cross the blood-brain barrier and directly act on the central nervous system. Although it has been proven to be relatively safe, currently, the randomized controlled trials related to magnesium L - threonate have only confirmed its improvement effects on pain and cognitive function \[23,24\], and the research on its effect on improving overall menopausal symptoms is rare. This study aims to deeply explore whether magnesium L-threonate can effectively improve the menopausal symptoms of perimenopausal women and improve their quality of life. Participants will be randomly divided into an intervention group and a control group, and medications are administered according to the following protocols: Intervention group: Magnesium L-threonate, 1740 mg, taken orally, twice a day, for 8 weeks. Control group: Placebo of magnesium L-threonate, 1740 mg, taken orally, twice a day, for 8 weeks. The face-to-face questionnaire surveys, physical examinations, and biological sample collections will be conducted during the study screening period and at the end of the study (8 weeks completed) ± 1 day. The online questionnaire surveys will be carried out on the 3rd week ± 1 day, 5th week ± 1 day, and 7th week ± 1 day of the intervention period.

Conditions

Interventions

TypeNameDescription
DRUGMagnesium-L-ThreonateMagnesium L-threonate, 1740 mg, taken orally, twice a day, for 8 weeks.
DRUGPlaceboPlacebo, 1740 mg, taken orally, twice a day, for 8 weeks.

Timeline

Start date
2025-05-15
Primary completion
2025-09-30
Completion
2025-12-30
First posted
2025-05-07
Last updated
2025-05-07

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06959745. Inclusion in this directory is not an endorsement.