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Recruiting NCT07526831

NCT07526831 Comparison of the Analgesic Efficacy of Adductor Canal Block and Combined Adductor Canal Block Plus IPACK Block in Knee Surgery

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Clinical Trial Summary
NCT ID NCT07526831
Status Recruiting
Phase
Sponsor TC Erciyes University
Condition Knee Arthroplasty, Total
Study Type OBSERVATIONAL
Enrollment 60 participants
Start Date 2026-04-15
Primary Completion 2028-04-15

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Adductor Canal Block Group (Group I)Adductor Canal + iPACK Block Group (Group II)"

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 60 participants in total. It began in 2026-04-15 with a primary completion date of 2028-04-15.

⚠ 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

To evaluate the effectiveness of Adductor Canal Block and combined Adductor Canal plus IPACK block in reducing postoperative pain and analgesic requirements in patients undergoing knee surgery.

Eligibility Criteria

Inclusion Criteria: * ASA (American Society of Anesthesiologists) I- ASA II-ASA III Patients Exclusion Criteria: * history of allergy to the study medication * refusal to participate

Contact & Investigator

Central Contact

Sibel Pehlivan, DR

✉ Sibelpehlivan@erciyes.edu.tr

📞 0905052532919

Principal Investigator

Sibel Pehlivan

STUDY DIRECTOR

Erciyes Üniversitesi

Frequently Asked Questions

Who can join the NCT07526831 clinical trial?

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

Is NCT07526831 currently recruiting?

Yes, NCT07526831 is actively recruiting participants. Contact the research team at Sibelpehlivan@erciyes.edu.tr for enrollment information.

Where is the NCT07526831 trial being conducted?

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

Who is sponsoring the NCT07526831 clinical trial?

NCT07526831 is sponsored by TC Erciyes University. The principal investigator is Sibel Pehlivan at Erciyes Üniversitesi. The trial plans to enroll 60 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: September 2026  ·  Data Methodology