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Sulpiride Versus Placebo for Reducting Hot Flushes During Climacteric

Sulpiride Versus Placebo for Reducting Hot Flushes During Climacteric: a Double-blind Randomized Clinical Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02749747
Enrollment
28
Registered
2016-04-25
Start date
2014-06-30
Completion date
2017-12-31
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hot Flashes, Menopausal Syndrome

Keywords

Menopause, nonhormonal treatment, sulpiride

Brief summary

* Introduction: Estrogen hormonal therapy associated or not with progestagen is the standard therapy for the treatment of hot flushes. However some women are not candidates for hormone replacement therapy for medical reasons or for choice. * Main goal: Reducing the number of hot flushes per week * Materials and Methods: A double-blind sulpiride versus placebo that includes selected randomized patients which show symptoms of menopause. The study will be conducted at HC Porto Alegre (Brazil) for 8 weeks of intervention. The expected result is a significant reduction in the number of hot flushes/day evaluated by daily questionnaires

Detailed description

It will be held 4 visits. The V0 (first one) to implement the consent form, review the inclusion and exclusion criteria and laboratory exams and deliver the diary book of hot flushes. The V1 (second visit) randomization and provide medication for the first 30 days. The V2 (third visit) to make the record diary of hot flushes already filled, to deliver new specifications and to provide medication for the last 30 days. The V3 (fourth visit) to evaluate the record diary of hot flushes already completed and to make a final evaluation of the study.

Interventions

DRUGSulpiride use

50mg sulpiride once a day use for 60 days

DRUGPlacebo

50mg placebo once a day use for 60 days

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Healthy women in postmenopausal women with at least five moderate to intense hot flushes per day

Exclusion criteria

* Use of hormone replacement therapy or psychiatric drugs for at least 3 months * Hypersensitivity to sulpiride * Current or history of prolactin dependent tumor * Treating breast cancer or treated * Diagnosed or suspected pheochromocytoma * Current use of levodopa * Abnormal heart rhythm (QT prolongation, bradycardia low 55 beats per minute) * Hypokalemia and other serious electrolyte disturbances * Current or treated stroke * Pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Number and severity records of hot flushesFrom baseline to eight weeksDaily diary of symptoms

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026