# Clinical Efficacy of Changing the InterStim® Parameters in Patients With Interstitial Cystitis/Painful Bladder Syndrome

> **NCT01312259** · PHASE4 · UNKNOWN · sponsor: **Pelvic and Sexual Health Institute** · enrollment: 72 (estimated)

## Conditions studied

- Painful Bladder Syndrome
- Interstitial Cystitis
- Pelvic Floor; Insufficiency
- Bowel Dysfunction
- Sexual Dysfunction
- Pelvic Floor; Incompetency

## Interventions

- **OTHER:** Changing the Interstim parameter of '' Frequency" in patients with Interstitial Cystitis

## Key facts

- **NCT ID:** NCT01312259
- **Lead sponsor:** Pelvic and Sexual Health Institute
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2011-04
- **Primary completion:** 2017-04
- **Final completion:** 2018-04
- **Target enrollment:** 72 (ESTIMATED)
- **Last updated:** 2014-04-29


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01312259

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01312259, "Clinical Efficacy of Changing the InterStim® Parameters in Patients With Interstitial Cystitis/Painful Bladder Syndrome". Retrieved via AI Analytics 2026-06-23 from https://api.ai-analytics.org/clinical/NCT01312259. Licensed CC0.

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