# Clinical Study for the Evaluation of the Efficiency of a Device for the Diagnosis of an Internal Rectal Prolapse, a Pelvic Floor Ptosis and for the Determination of an Internal Hernia Into the Douglas Pouch

> **NCT00836680** · NA · UNKNOWN · sponsor: **Gerhard Pejcl Medizintechnik GmbH** · enrollment: 15 (estimated)

## Conditions studied

- Internal Rectal Prolapse
- Pelvic Floor Ptosis
- Internal Hernia Into the Douglas Pouch

## Interventions

- **DEVICE:** Colorectal Stent

## Key facts

- **NCT ID:** NCT00836680
- **Lead sponsor:** Gerhard Pejcl Medizintechnik GmbH
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2009-01
- **Primary completion:** 2009-05
- **Final completion:** 2009-06
- **Target enrollment:** 15 (ESTIMATED)
- **Last updated:** 2009-02-04


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00836680

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00836680, "Clinical Study for the Evaluation of the Efficiency of a Device for the Diagnosis of an Internal Rectal Prolapse, a Pelvic Floor Ptosis and for the Determination of an Internal Hernia Into the Douglas Pouch". Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/clinical/NCT00836680. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*