Feasibility of using a semi standardised prognostic protocol in homeopathic treatment for premenstrual syndrome/symptoms: pilot study for a pragmatic randomised trial

Feasibility of using a semi standardised prognostic protocol in homeopathic treatment for premenstrual syndrome/symptoms: pilot study for a pragmatic randomised trial - Homeopathic treatment of premenstrual syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON31118

Enrollment

Registered

2007-09-14

Start date

2007-07-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

PMS premenstrual syndrome

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Sex: female Age: 18-50 Diagnosis premenstrual syndrome/symptoms

Exclusion criteria

Exclusion criteria: pregnant or wanting to get pregnant use of hormones, excl. contraceptive pill use of antidepressants recent homeopathic treatment (within the last two months)

Design outcomes

Primary

Measure	Time frame
Changes of complaints and general well being, measured separately by the AGOS, an adjusted GHHOS-scale, a nine point Likert scale. Changes in premenstrual symptoms will be measured by mean PMS-diary scores of the last two weeks before the menstruation. The PMS diary is a modifcation of the MDQ.	—

Secondary

Measure	Time frame
Days with use of conventional medicines and number of medicines, days with absence from work	—

Countries

Netherlands

Outcome results