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NCT03673488UNKNOWNanonymous

Prospective Study to Evaluate Use of TephaFLEX™ Sling Implanted Via a Retropubic Mid-urethral Sling Procedure for Treatment of Women With Stress Urinary Incontinence

Sponsor

Source record

Pelvic Floor Research Foundation of South Africa

Phase

Source record

Observational

Modality

AI-normalized

medical device

Target

AI-normalized

Stress Urinary Incontinence

Indication / condition

AI-normalized

Stress Urinary Incontinence

Intervention

Source record

TephaFlex™ mid-urethral sling

Source & freshness

Source record

NCT ID

NCT03673488

Original source

ClinicalTrials.gov

Source last updated

Sep 17, 2018

Ingested at

May 30, 2026

Internal sync

Jun 05, 2026

Model version

trialsignal-ai-v1

Normalized confidence

88%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT03673488

Title

Prospective Study to Evaluate Use of TephaFLEX™ Sling Implanted Via a Retropubic Mid-urethral Sling Procedure for Treatment of Women With Stress Urinary Incontinence

Sponsor

Pelvic Floor Research Foundation of South Africa

Status

UNKNOWN

Phase

Observational

Condition raw

Stress Urinary Incontinence

Condition normalized

Stress Urinary Incontinence

Modality raw

Stress Urinary Incontinence

Modality normalized

medical device

Target raw

Stress Urinary Incontinence

Target normalized

Stress Urinary Incontinence

Interventions

TephaFlex™ mid-urethral sling

Public preview

Source record

The study evaluates the safety and efficacy of the TephaFLEX sling, a bioresorbable device made from poly-4-hydroxybutyrate (P4HB), for treating stress urinary incontinence in women. The trial aims to establish the feasibility of using a non-permanent mesh as an alternative to traditional polypropylene slings, which are associated with complications.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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TrialSignal

Clinical trial intelligence report

Prospective Study to Evaluate Use of TephaFLEX™ Sling Implanted Via a Retropubic Mid-urethral Sling Procedure for Treatment of Women With Stress Urinary Incontinence

Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.

Generated

Jun 13, 2026

NCT ID

NCT03673488

Status

UNKNOWN

Phase

Observational

Sponsor

Pelvic Floor Research Foundation of South Africa

Executive brief

Investment-Ready Snapshot

The study evaluates the safety and efficacy of the TephaFLEX sling, a bioresorbable device made from poly-4-hydroxybutyrate (P4HB), for treating stress urinary incontinence in women. The trial aims to establish the feasibility of using a non-permanent mesh as an alternative to traditional polypropylene slings, which are associated with complications.

Source & freshness

Provenance

SourceClinicalTrials.gov
Source updatedSep 17, 2018
Internal syncJun 05, 2026
Model versiontrialsignal-ai-v1

https://clinicaltrials.gov/study/NCT03673488

Indication

Stress Urinary Incontinence

Modality

medical device

Target

Stress Urinary Incontinence

Intervention

TephaFlex™ mid-urethral sling

Source record

Protocol Description

Detailed source ingestion pending.

Source record

Outcome Measures

Detailed source ingestion pending.

Source record

Eligibility

Detailed source ingestion pending.

AI analysis

Known Results And Readout Context

Detailed source ingestion pending.

IP intelligence

Patent And IP Landscape

Detailed source ingestion pending.

Source record

Contacts

Detailed source ingestion pending.