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Completed

NCT Number: NCT06192641

Melatonin Use in Patients With Climacterious Symptoms in the Perimenopause

Menopause is defined as the absence of menstruation for 12 months without a pathological cause and it is marked by physical fluctuations and biological changes that can impact women's quality of life. During the perimenopause and menopause transition period, women may experience a variety of changes, including menstrual cycle irregularity and climacteric symptoms. Treatment to relieve symptoms may include hormonal and non-hormonal options, such as behavioral therapies, medications and low-dose hormonal therapies. The objective of this study will be to evaluate the effect of melatonin in women with perimenopausal symptoms. This is a double-blind, placebo-controlled randomized clinical trial research, where perimenopausal women will be interviewed, who will answer questionnaires, and will use melatonin/placebo for a period of 30 days, before and after, they will be asked about possible changes during treatment, such as mood changes, drowsiness, dizziness, headaches or allergic reactions. It is hoped that with this study, the effect of melatonin in women on climacteric symptoms during the perimenopausal period will be understood.

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Key information

Age range

45 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Gabriela Laste

Lajeado, Rio Grande do Sul, 95900-000, Brazil

About this study

This is a randomized, double-blind, parallel, placebo-controlled clinical trial. 40 patients will be recruited to participate in the study, 20 of whom will receive the treatment and 20 will receive the placebo for a period of 30 days.Before and after, they will be asked about possible changes during treatment, such as mood changes, drowsiness, dizziness, headaches or allergic reactions.

The study will be carried out at the São Cristóvão Basic Health Unit in Lajeado - RS. The research and invitation to participate will also be publicized through the University of Vale do Taquari's social media, through an informative/explanatory text. Data collection from these participants will be carried out at their homes or in a location that suits them best by arrangement. If the participant has travel expenses for their participation, travel/transportation costs will be reimbursed within the project budget, which will be the responsibility of the responsible researcher.

The study protocol was submitted and approved by the Univates Health Research Ethics Committee by CAAE: 70400923.9.0000.5310 and opinion no.: 6.131.475.

For statistical analyzes the statistical program JAMOVI (Version 2.3) [Computer Software] (2022) and R Core Team (2021) will be used. The Kolmogorov Smirnov and Shapiro-Wilk Test will be used to verify the normality of the data. Non-parametric samples will be analyzed using the Mann-Whitney U test and parametric t-test. Continuous variables will be presented as mean±SD. The number and percentage will be presented as n (%), and numerical data will be analyzed using the Chi-square test (χ²) and/or Fisher's exact test. The Confidence Interval value (IC95%) will be provided. The value of p<0.05 will be considered statistically significant.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

- Being female and in peri-menopause, experiencing an irregular menstrual cycle, having had at least one menstrual period in the last 6 months.

  • Age 45 years or older
  • Be literate

Exclusion criteria

-History of alcohol or other substance abuse in the last 6 months

  • Use of hormonal therapy;
  • Neurological disease;
  • Oncological disease;
  • Ischemic heart disease;
  • Liver failure;
  • Renal insufficiency;
  • Use of central nervous system medications (antidepressants, anticonvulsants, antipsychotics and benzodiazepines)

Treatment and study plan

Melatonin 3 MG

Drug

patients received 3 mg melatonin in capsule or placebo (capsule identical to the treatment, both in color, taste, odor and shape, composed of cellulose and indigestible fiber) (PALMER, 2020). (GOLTZMAN, 2021) for 30 days (Treister-Goltzman; Peleg, 2021) They will be instructed to ingest melatonin once a day, at night, one hour before bed (PALMER, et al. 2020).

Other names: melatonin

Primary outcomes

  1. Menopause rating scale

    Time frame: one month

    Menopause scale, 0-44, higher score worse outcome

Secondary outcomes

  1. Beck Depression Inventory II

    Time frame: one month

    Level of depressive symptoms, 0-63, higher score worse outcome. Score 16 is considered depression.

  2. Pittsburgh Sleep Quality Index

    Time frame: one month

    Sleep quality, 0-20, higher score worse sleep

  3. Visual Analog Pain Scale

    Time frame: daily for one month

    pain scale, can vary from zero (no pain) to 100 mm (worst possible pain)

  4. Hamilton scale

    Time frame: one month

    anxiety rating scale, 0-56, >30 severe anxiety.

  5. Visual analogue scale of sleep

    Time frame: daily for one month

    sleep scale, varies from worst possible (0) to best possible (10 cm)

Sponsors and collaborators

Lead sponsor

Univates

Other

Collaborators

  • Aline Patrícia Brietzke
  • Ana Paula Costella

Registry information

Official study title

Benefits of Melatonin Use in Patients With Climacterious Symptoms in the Perimenopause: Randomized, Double-blind, Placebo-controlled Clinical Trial

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jan 5, 2024
Registry last updated
Nov 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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