Last reviewed · How we verify
NCT05608655: DELTA
DKutting Balloon Versus Chocolate Balloon to Treat Femoral and Popliteal Artery Stenosis
NA trial testing DKutting LL balloon in Femoral Artery Stenosis in 188 participants. Completed in 4 February 2024.
10 January 2024
Quick facts
| Lead sponsor | DK Medical Technology (Suzhou) Co., Ltd. |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 188 |
| Start date | 27 December 2022 |
| Primary completion | 10 January 2024 |
| Estimated completion | 4 February 2024 |
| Sites | 14 locations across China |
Drugs / interventions tested
- DKutting LL balloon
- Chocolate balloon
Conditions studied
- Femoral Artery Stenosis — all drugs for Femoral Artery Stenosis →
- Popliteal Artery Stenosis — all drugs for Popliteal Artery Stenosis →
Sponsor
DK Medical Technology (Suzhou) Co., Ltd.
Who can join
Adults 18 to 80, any sex, with Femoral Artery Stenosis or Popliteal Artery Stenosis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A Multicenter, Prospective, Randomized Controlled Trial to Evaluate the Efficacy and Safety of DKutting Balloon Versus Chocolate Balloon in the Treatment of Femoral and Popliteal Artery Stenosis
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT05608655
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other DK Medical Technology (Suzhou) Co., Ltd. trials
Trials by the same sponsor.
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- NCT03376646 — A Safety and Efficacy Study of Dissolve™ in Treatment of Coronary Small Vessel Disease · NA · completed
- NCT03373695 — A Safety and Efficacy Study of Dissolve™ in Treatment of Coronary In-stent Restenosis · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05608655 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by DK Medical Technology (Suzhou) Co., Ltd.
- Last refreshed: 20 February 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05608655.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing