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AzTrials

Pharmaceutical sponsor

Aesculap AG Clinical Trials

Studies where Aesculap AG is the lead sponsor: its pipeline by phase, what is enrolling now and where. Studies it supports as a collaborator are in the search.

105 registered studies

In numbers

Open to volunteers
20
Active
29
With results posted
1
All registered
105

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 20
  • Subdural Hematoma, Subdural Hematoma, Chronic

    Study On Histoacryl Used For Embolization Of Middle Meningeal Artery (MMA) In Chronic Subdural Hematoma (CSDH)

    • Recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    The aim of the study is to proof the effectiveness of Histoacryl® on preventing recurrence or progression of subdural hematoma after embolization of the middle meningeal artery.

    Trial name
    HARMONY (NCT07258069)
    Testing
    Histoacryl®
    Where
    6 sites in Japan
    Volunteers
    178 people
    Sponsor
    Aesculap AG
    Can I take part? HARMONY
  • Arthroplasty, Arthroplasty Replacement, Knee

    oneKNEE - Prospective, Non-interventional, Multicenter PMCF-Study

    • Not yet recruiting
    • Age: 18 to 79 years
    • Observational study
    • Medical device

    Safety and Clinical Performance in terms of clinical outcome of oneKNEE® (total knee arthroplasty TKA), evaluated 2 years after implantation.

    Conditions
    Arthroplasty, Arthroplasty Replacement, Knee, Prosthetic Joint Infections of Knee, TKA Outcomes
    Trial name
    oneKNEE (NCT07682909)
    Testing
    oneKNEE®
    Volunteers
    1,020 people
    Sponsor
    Aesculap AG
    Can I take part? oneKNEE
  • Primary Osteoarthritis, Cartilage Degeneration

    DEXA Bone Density Analysis of the CoreHip® Prosthesis System

    • Not yet recruiting
    • Age: 35 to 85 years
    • Medical device

    The goal of this interventional post-market follow-up study is to evaluate radiological changes in the diaphyseal bone density (Gruen Zones 3 and 4) within 24 months postoperative in patients treated with CoreHip® primary…

    Conditions
    Primary Osteoarthritis, Cartilage Degeneration, Osteoarthritis, Hip, Inflammatory Arthritis
    Trial name
    CODEX (NCT06632301)
    Testing
    Primary hip replacement with cementless stem
    Where
    Germany
    Volunteers
    40 people
    Sponsor
    Aesculap AG
    Can I take part? CODEX
  • Gonarthritis, Degenerative Disease

    Clinical Performance and Safety of the Unicompartmental Univation® XF Pro Implant

    • Recruiting
    • Age: 18 to 75 years
    • Observational study
    • Medical device

    The study is designed as a prospective, observational, mid-term, multi-center follow-up study. It is planned to include 150 patients from 4 different study centres in Germany.

    Trial name
    UNI_XF_PRO (NCT06657248)
    Testing
    univation® XF Pro
    Where
    4 sites in Germany
    Volunteers
    150 people
    Sponsor
    Aesculap AG
    Can I take part? UNI_XF_PRO
  • Gingivitis, Gingival Diseases

    NOVOSYN® Quick Versus MONOSYN® Quick Suture Material in Resective Periodontal Surgery

    • Recruiting
    • Age: 18 years and older
    • Medical device

    The aim of this study is to prove that Novosyn Quick and Monosyn Quick are equivalent in early wound healing in adult patients undergoing resective periodontal surgery.

    Conditions
    Gingivitis, Gingival Diseases, Periodontal Diseases
    Trial name
    NOQMOQS (NCT05813236)
    Testing
    Novosyn® in resective periodontal surgery, Monosyn® in resective periodontal surgery
    Where
    Spain
    Volunteers
    84 people
    Sponsor
    Aesculap AG
    Can I take part? NOQMOQS
  • Hemorrhage, Gastrointestinal Hemorrhage

    HISTOACRYL® Used for Embolization of Thoracoabdominal Artery Bleeding

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    This observational study will collect information from adult patients in Japan who are treated with Histoacryl® to stop bleeding from arteries in the chest or abdomen, in order to better understand how well the treatment works…

    Conditions
    Hemorrhage, Gastrointestinal Hemorrhage, Hemoptysis, Postpartum Hemorrhage
    Trial name
    HEAL (NCT07753005)
    Testing
    Embolization therapy
    Where
    11 sites in Japan
    Volunteers
    176 people
    Sponsor
    Aesculap AG
    Can I take part? HEAL
  • Bone Regeneration

    Performance and Safety of Lyoplant® in Guided Bone Regeneration (GBR) in Oral Surgery

    • Recruiting
    • Age: 18 years and older
    • Surgery or procedure

    Guided Bone Regeneration (GBR) is a well-established surgical technique that employs barrier membranes to ensure the stability of bone augmentation material while preventing the infiltration of soft tissue, thereby facilitating…

    Trial name
    LyOral (NCT06732167)
    Testing
    GBR Lyoplant, GBR Bio-Gide
    Where
    2 sites in Spain
    Volunteers
    68 people
    Sponsor
    Aesculap AG
    Can I take part? LyOral
  • Spine Fracture, Degenerative Disc Disease

    Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical

    • Recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    Multicenter Post market clinical follow-up Study on the Safety and Performance of Ennovate® Cervical - Prospective, pure data collection of all Ennovate Cervical patients in Total Indications

    Conditions
    Spine Fracture, Degenerative Disc Disease, Spinal Instability, Spinal Tumor
    Trial name
    CERISE (NCT05296889)
    Testing
    posterior stabilization for the cervical spine
    Where
    4 sites in Germany
    Volunteers
    200 people
    Sponsor
    Aesculap AG
    Can I take part? CERISE
  • Anastomotic Leak, Colon Cancer

    Leakage Rate of Ileo-COlic Sutured Anastomosis After Right Hemicolectomy

    • Recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    The primary aim of the study is to show that the ileo-colic anastomosis leakage rate until the first 30 days after surgery using MonoPlus® suture material for anastomosis construction after right hemicolectomy is not inferior to…

    Conditions
    Anastomotic Leak, Colon Cancer, Right Hemicolectomy
    Trial name
    LICOSARH (NCT07132970)
    Testing
    Monoplus Suture Material
    Where
    4 sites in Germany
    Volunteers
    249 people
    Sponsor
    Aesculap AG
    Can I take part? LICOSARH
  • Abnormal Uterine Bleeding, Endometriosis

    Performance of SYMMCORA® vs. V-Loc® Suture Material in Patients Undergoing Laparoscopic Total Hysterectomy

    • Recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    The aim of this study is to show the superiority of the new unidirectional barbed suture (SYMMCORA® mid-term, unidirectional) to conventional suture material in terms of time to perform the vaginal cuff closure during gynecologic…

    Conditions
    Abnormal Uterine Bleeding, Endometriosis, Uterine Prolapse, Uterine Cancer
    Trial name
    BARHYSTER (NCT06024109)
    Testing
    Closure of the Vaginal Cuff after Total Hysterectomy
    Where
    2 sites in Germany, Spain
    Volunteers
    132 people
    Sponsor
    Aesculap AG
    Can I take part? BARHYSTER

Completed, with results posted

All 1

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