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Recruiting NCT07651735

NCT07651735 Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Primary Hip Prosthesis System

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Clinical Trial Summary
NCT ID NCT07651735
Status Recruiting
Phase
Sponsor TIPMED Medical Device Manufacturing Ltd. Co.
Condition Total Hip Arthroplasty (THA)
Study Type OBSERVATIONAL
Enrollment 101 participants
Start Date 2024-03-12
Primary Completion 2028-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Tipmed™ Primary Hip Prosthesis System

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 101 participants in total. It began in 2024-03-12 with a primary completion date of 2028-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is a multicenter, prospective, observational, post-market clinical follow-up (PMCF) study designed to evaluate the safety and clinical performance of the Tipmed™ Primary Hip Prosthesis System in adult subjects undergoing primary hip arthroplasty. The study aims to gather real-world clinical evidence on the 24-month post-operative safety profile, potential complications, and functional outcomes of the device during routine clinical practice.

Eligibility Criteria

Inclusion Criteria: * Individuals aged 18 years and older, * Male or female participants, * Subjects who have undergone Primary Hip Arthroplasty (either total or partial) for any indication, * Subjects in whose surgical procedure the Tipmed™ Primary Hip Prosthesis System components were utilized. * Subjects who are not legally restricted (e.g., military personnel, convicts, or individuals under legal guardianship). * Subjects who have voluntarily signed the written Informed Consent Form (ICF). Exclusion Criteria: * Subjects currently participating in any other interventional clinical trial.

Contact & Investigator

Central Contact

Yasemin Önel, Sponsor Rep

✉ yaseminonel@tipmed.com

📞 +90 232 479 33 22

Principal Investigator

Ahmet Karakaşlı, Professor

STUDY DIRECTOR

Dokuz Eylul University

Frequently Asked Questions

Who can join the NCT07651735 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Total Hip Arthroplasty (THA). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07651735 currently recruiting?

Yes, NCT07651735 is actively recruiting participants. Contact the research team at yaseminonel@tipmed.com for enrollment information.

Where is the NCT07651735 trial being conducted?

This trial is being conducted at Balıkesir, Turkey (Türkiye), Balıkesir, Turkey (Türkiye), Izmir, Turkey (Türkiye), Izmir, Turkey (Türkiye).

Who is sponsoring the NCT07651735 clinical trial?

NCT07651735 is sponsored by TIPMED Medical Device Manufacturing Ltd. Co.. The principal investigator is Ahmet Karakaşlı, Professor at Dokuz Eylul University. The trial plans to enroll 101 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology