# A Feasibility Study Designed to Assess the Efficacy of the ActiLady Device in Adult Female Subjects With Dysmenorrhea

> **NCT00855829** · PHASE1 · COMPLETED · sponsor: **Hadassah Medical Organization** · enrollment: 24 (estimated)

## Conditions studied

- Dysmenorrhea

## Interventions

- **DEVICE:** Miniature Actilady device active
- **DEVICE:** Miniature Actilady device not active

## Key facts

- **NCT ID:** NCT00855829
- **Lead sponsor:** Hadassah Medical Organization
- **Sponsor class:** OTHER
- **Phase:** PHASE1
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2010-05
- **Primary completion:** 2013-05
- **Final completion:** 2013-10
- **Target enrollment:** 24 (ESTIMATED)
- **Last updated:** 2013-11-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00855829

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00855829, "A Feasibility Study Designed to Assess the Efficacy of the ActiLady Device in Adult Female Subjects With Dysmenorrhea". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT00855829. Licensed CC0.

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