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Evaluation of treatment in menopausal wemon with hotflashes

Study the effect of different doses of piascledine on hot flashing of menopausal women in Jahrom city.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015051821653N3
Enrollment
69
Registered
2015-06-15
Start date
2015-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

menopausal. Menopausal and other perimenopausal disorders

Interventions

Intervention 1: Control group: no intervention will take on them and do not take piascledine. Intervention 2: Case group (number1): will take one piascledine 300 mg pill daily, during three months. p
Treatment - Drugs
Case group (number2): will take two piascledine 300 mg pill daily, during three months. piascledine should be used with food and a glass of water.
Control group: no intervention will take on them and do not take piascledine.
Case group (number1): will take one piascledine 300 mg pill daily, during three months. piascledine should be used with food and a glass of water.

Sponsors

Jahrom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: menopausal women that have not menstural cycle among last one year; having hotflashes according to kuperman index; do not take another treatment such as hormone replacement, food supplements and plantal drugs. Exclusion criteria: nonmenopausal women; do not have hotflashing according to kuperman index; taking hormone replacement therapy; women can not continue using drug beacuse of gastrointestinal complication or other things.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hotflashes. Timepoint: Before intervention and in first, second and third month after intervention. Method of measurement: Scoring is from 0 to 3 according to: not at all (0), a little (1), quite a bit (2), Extremely (3). then the hotflashes score will multiply to 4.;Paraesthesia. Timepoint: Before intervention and in first, second and third month after intervention. Method of measurement: Scoring is from 0 to 3 according to: not at all (0), a little (1), quite a bit (2), Extremely (3). then the paraesthesia score will multiply to 2.;Iinsomnia. Timepoint: Before intervention and in first, second and third month after intervention. Method of measurement: Scoring is from 0 to 3 according to: not at all (0), a little (1), quite a bit (2), Extremely (3). then the insomnia score will multiply to 2.;Nervousness. Timepoint: Before intervention and in first, second and third month after intervention. Method of measurement: Scoring is from 0 to 3 according to: not at all (0), a little (1), quite a bit (2), Extremely (3). then the nervousness score will multiply to 2.;Melancholia. Timepoint: Before intervention and in first, second and third month after intervention. Method of measurement: Scoring is from 0 to 3 according to: not at all (0), a little (1), quite a bit (2), Extremely (3). then the melancholia score will multiply to 1.;Vertigo. Timepoint: Before intervention and in first, second and third month after intervention. Method of measurement: Scoring is from 0 to 3 according to: not at all (0), a little (1), quite a bit (2), Extremely (3). then the vertigo score will multiply to 1.;Weakness. Timepoint: Before intervention and in first, second and third month after intervention. Method of measurement: Scoring is from 0 to 3 according to: not at all (0), a little (1), quite a bit (2), Extremely (3). then the weakness score will multiply to 1.;Arthralgia or myalgia. Timepoint: Before intervention and in first, second and third month after intervention. Method of m

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDoctor Athar Rasekh Jahromi

Jahrom University of Medical Sciences

drrasekh@yahoo.comm.zareian91@yahoo.com+98 715426602

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026