Coronary Restenosis clinical trials
The registry lists 107 studies for Coronary Restenosis across more than 10 countries. 10 are recruiting or about to start. 30 of them are mainly about Coronary Restenosis (how this is decided). Per ClinicalTrials.gov, last updated 2026-10-20.
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Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
Now Active, not recruiting
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Who runs them
Abbott Medical Devices (39) · Peking Union Medical College Hospital (4) · Foundation of Cardiovascular Research and Education Enschede (4) · Deutsches Herzzentrum Muenchen (3) · Thorax Centrum Twente (2) · Luzerner Kantonsspital (2) · Biosensors Europe SA (2) · University Hospital, Saarland (2)
What is being tested here
Drugs under test in Coronary Restenosis studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
| Drug | Open | Phase 3 | All |
|---|---|---|---|
| Sirolimus | 0 | 0 | 2 |
| Albumin-Bound Paclitaxel | 0 | 0 | 1 |
| Paclitaxel | 0 | 0 | 1 |
| Insulin | 0 | 0 | 1 |
| Thalidomide | 0 | 0 | 1 |
| Pioglitazone | 0 | 1 | 1 |
| Celecoxib | 0 | 0 | 1 |
| Everolimus | 0 | 1 | 1 |
Drug classes tested here mTOR inhibitors 3
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 3
- Dec 2026Clinical Features, Current Treatment and Clinical Outcomes in Patients With INR-CAD: a Cohort Study · Peking Union Medical College Hospital
- Dec 2026SIROOP Registry - a Prospective Registry Study to Evaluate the Outcomes of Coronary Artery Disease Patients Treated with SIROlimus or Paclitaxel Eluting Balloon Catheters · Luzerner Kantonsspital
- Jan 2027The PICCOLETO XIII REVEAL-DCB Cohort A Study · Fondazione Ricerca e Innovazione Cardiovascolare ETS
Who these studies take
Of the 8 Coronary Restenosis studies recruiting now, 7 (88%) set no upper age limit and 1 (13%) stop at 75 or younger. 0 (0%) take children under 18. 0 (0%) are for women only and 0 (0%) for men only; 0 (0%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 0 (0%) | 0 (0%) |
| 18 | 7 (88%) | 7 (88%) |
| 30 | 7 (88%) | 7 (88%) |
| 40 | 7 (88%) | 7 (88%) |
| 50 | 8 (100%) | 8 (100%) |
| 65 | 7 (88%) | 7 (88%) |
| 75 | 7 (88%) | 7 (88%) |
| 85 | 7 (88%) | 7 (88%) |
Across all 107 studies, recruiting or not: 7% stop at 75 or younger and 1% at 65; 7% take children; 2% are for women only and 0% for men only; 1% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
How long Coronary Restenosis studies take
Of 13 interventional studies with no phase under Coronary Restenosis, half reached primary completion within 44 months of starting, counting those still running.
| Start to primary completion | Every sponsor | Industry | Non-industry |
|---|---|---|---|
| Interventional, no phase | 44 mo28–61 · 13 studies | — | — |
Each figure is the month by which half the studies had reached primary completion, with the range in which the middle half did. Studies still running count until their last registry update; studies that stopped early are left out. Phase 1 includes early phase 1; observational means prospective or not stated, as retrospective and cross-sectional studies date a window of data rather than a study. How these figures are worked out
What changed recently
From the registry's own updates since Oct 14, 2026.
Results posted1
- SELUTION SLR™ 014 In-stent RestenosisOct 20, 2026NCT04280029
Studies
Recruiting first, then most recently updated. Showing 50 of 107. Browse all 107 → or search them.
- Abbott Vascular Medical Device RegistryRecruitingNCT0457366014 countries
- The PICCOLETO XIII REVEAL-DCB Cohort A StudyNot yet recruitingNCT07868523
- Restrospective Analysis of MACE in Patients Treated With Drug-elluting Balloons.RecruitingNCT069722251 country
- Disease Characteristics of R-CADNot yet recruitingNCT07239921
- Disease Characteristics of IR-CAD: a Case-control StudyRecruitingNCT060072481 country
- Efficacy and Safety of Comprehensive Treatment in Patients With IR-CAD: a Self-controlled Cohort StudyRecruitingNCT058604001 country
- Clinical Features, Current Treatment and Clinical Outcomes in Patients With INR-CAD: a Cohort StudyRecruitingNCT068454101 country
- Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent Implantation or Drug-coated Balloon Angioplasty According to Neointima Morphology in Drug-eluting Stent Restenosis 5RecruitingNCT05544864Not applicable2 countries
- COMPLEX Registry - a Prospective COhort Study to Describe the Management and Outcomes of Patients Presenting with CompLEX and Calcified Coronary Artery DiseaseRecruitingNCT060756021 country
- SIROOP Registry - a Prospective Registry Study to Evaluate the Outcomes of Coronary Artery Disease Patients Treated with SIROlimus or Paclitaxel Eluting Balloon CathetersRecruitingNCT049886851 country
- SELUTION SLR™ 014 In-stent RestenosisActive, not recruitingNCT04280029Not applicable7 countries
- Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xience Sierra Everolimus-eluting StentsCompletedNCT044753801 country
- AnGiographic Performance With A Sirolimus-elutiNG Balloon in the TrEatment of De Novo CoronaRy Artery DiseaseCompletedNCT05471245Not applicable1 country
- STAR and Deferred Stenting StudyCompletedNCT05089864Not applicable1 country
- Concordance Between FFR and iFR for the Assessment of Intermediate Lesions in the Left Main Coronary Artery. A Prospective Validation of a Default Value for iFRActive, not recruitingNCT037676211 country
- DEB Versus 2nd Generation DES in Patients With In-Scaffold Restenosis of Bioresorbable Vascular ScaffoldWithdrawnNCT03074305Not applicable1 country
- BIOFLOW-SV All Comers RegistryTerminatedNCT036009481 country
- XIENCE V® USA Dual Antiplatelet Therapy (DAPT) CohortCompletedNCT01106534Phase 41 country
- Absorb IV Randomized Controlled TrialCompletedNCT02173379Not applicable5 countries
- ABSORB III Randomized Controlled Trial (RCT)CompletedNCT01751906Not applicable2 countries
- Treatment of In-Stent Restenosis by Paclitaxel Coated PTCA Balloons (PACCOCATH - ISR I)CompletedNCT00106587Phase 1/21 country
- Safety Study of a Bioresorbable Coronary StentCompletedNCT01262703Not applicable1 country
- Resveratrol Excipient Paclitaxel Coated Balloon for Coronary TreatmentWithdrawnNCT05093244Not applicable
- Treatment of In-Stent Restenosis 2 StudyCompletedNCT03667313Phase 31 country
- Restenosis in Coronary Stents And Cutaneous HEaLingStatus unknownNCT049153911 country
- Drug Eluting Balloon Angioplasty Versus Everolimus Platinum Chrome StentStatus unknownNCT05516446Not applicable1 country
- Comparison of BIOdegradable Polymer and DuRablE Polymer Drug-eluting Stents in an All COmeRs PopulaTion (BIO-RESORT)CompletedNCT01674803Not applicable1 country
- Physiology and Residual Ischemia After Percutaneous Coronary InterventionStatus unknownNCT044947501 country
- Treatment of Coronary In-stent Restenosis (ISR) by a Sirolimus Coated or a Paclitaxel Coated BalloonCompletedNCT03242096Not applicable2 countries
- PCI vs. CABG in UPLM-ISRCompletedNCT049689772 countries
- Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery LesionsCompletedNCT02229864Not applicable1 country
- SCRIPPS V: Intracoronary Brachytherapy for Recurrent Restenosis After Multiple Drug-Eluting StentsCompletedNCT00714545Phase 41 country
- Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the Endeavor Stent (Seaside)CompletedNCT00963781Phase 41 country
- AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japanese PopulationCompletedNCT01844284Not applicable1 country
- XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm StudyCompletedNCT018941521 country
- EXCEL Clinical TrialCompletedNCT01205776Not applicable1 country
- Comparison of Agent™ and SeQuent® Please Paclitaxel Coated Balloon Catheters in Coronary In-stent Restenosis (AGENT-ISR)CompletedNCT02151812Not applicable2 countries
- A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) System in Chinese Population ~ ABSORB CHINA Randomized Controlled Trial (RCT)CompletedNCT01923740Not applicable1 country
- ABSORB II Randomized Controlled TrialCompletedNCT01425281Not applicable1 country
- Compare the Efficacy and Safety of RESTORE DEB and SeQuent® Please in Chinese Patient With Coronary In-stent RestenosisCompletedNCT02944890Not applicable1 country
- Limus Eluted From A Durable Versus ERodable Stent CoatingCompletedNCT00389220Not applicable7 countries
- XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval, Single-Arm StudyCompletedNCT012490271 country
- ABSORB Clinical Investigation, Cohort BCompletedNCT00856856Not applicable8 countries
- Trial of a Novel Paclitaxel-coated Balloon With Citrate Excipient for Restenosis in -Limus Analogue DESCompletedNCT02367495Not applicable1 country
- To Study the Safety and Clinical Outcomes of the Absorb Bioresorbable Vascular Scaffold (BVS) System in Patients With de Novo Lesions in Previously Untreated VesselsCompletedNCT019775341 country
- Metal Allergy In-Stent Restenosis StudyStatus unknownNCT03588962Not applicable
- Retrospective Long-term Safety and Efficacy Study of the Beta-Cath(TM) 3.5F SystemStatus unknownNCT008521761 country
- Absorb BVS vs. Drug Coated Balloon for Treatment Of ISRSuspendedNCT02474485Not applicable1 country
- XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Protocol for JapanCompletedNCT010862281 country
- ABSORB EXTEND Clinical InvestigationCompletedNCT01023789Not applicable25 countries