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To compare the effect of vitamin B1 and vitamin C combination versus placebo in treatment of primary menstrual pain

Comparative Effectiveness of Vitamin B1 and Vitamin C Combination versus Placebo in Treatment of Primary Dysmenorrhoea A Randomized Double Blinded Placebo Controlled Study - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084190
Enrollment
84
Registered
2025-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: N71- Inflammatory disease of uterus, except cervix

Interventions

Intervention1: Benfotiamine tablets and Limcee tablets: T Benfotiamine 100MG, Per oral, Once a day, 3 months T Limcee 500MG, Per oral,Twice a day,3 months Control Intervention1: PLACEBO: EXCIPIENTS,

Sponsors

Kaviya V
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Single / not in a relationship Primary dysmenorrhoea moderate to severe in most of the cycles for minimum 6 months. No underlying gynaecology problem . Not on any drug intake. Should not take any other medication for dysmenorrhoea

Exclusion criteria

Exclusion criteria: Age less than 15 or more than 30 Secondary dysmenorrhoea or any other underlying gynaecology problem. Any abdominal / pelvic surgery . Smoking , drinking , taking hormonal drugs and ocps and severe mental tensions during research . Any kind of physical / mental disease

Design outcomes

Primary

MeasureTime frame
Effect on intensity and duration of pain by using VAS Effect on quality of life- QOL using WALIDD Score. Effect on vasoconstriction in uterine muscles by PI and RI of uterine vasculature.Timepoint: Pre- intervention 3 months post intervention

Secondary

MeasureTime frame
Effect on markers for primary dysmenorrhoea [ hsCRP,PGE2 ,PGF2alpha and ADMA). Drug complications, Amount of patient satisfactionTimepoint: pre - intervention 3 months post intervention

Countries

India

Contacts

Public ContactDr. V Kaviya

SRM Insitute of Science and Technology

dr.maitrayee@gmail.com

Outcome results

None listed

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