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Recruiting NCT06001736

NCT06001736 Utility of CC7 Transfer in Stroke Subtypes

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Clinical Trial Summary
NCT ID NCT06001736
Status Recruiting
Phase
Sponsor Dartmouth-Hitchcock Medical Center
Condition Stroke, Ischemic
Study Type INTERVENTIONAL
Enrollment 95 participants
Start Date 2022-03-13
Primary Completion 2027-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Contralateral C7 root transfer for the treatment of spastic hemiparesis.

Eligibility Fast-Check

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

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 95 participants in total. It began in 2022-03-13 with a primary completion date of 2027-03-01.

⚠ 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

The purpose of this study is to evaluate the limb functional improvement after contralateral C7 root transfer in stroke patients.

Eligibility Criteria

Inclusion Criteria: * History of ischemic or hemorrhagic stroke with resultant arm paresis that has ceased to improve within 1-5 years of rehabilitation. * baseline Fugl-Meyer score below 33 Exclusion Criteria: * pregnancy

Contact & Investigator

Central Contact

Lauren Sinks

✉ Lauren.J.Sinks@hitchcock.org

📞 (603) 653-9021

Principal Investigator

Jennifer Hong, Dr.

PRINCIPAL INVESTIGATOR

Dartmouth-Hitchcock Medical Center

Frequently Asked Questions

Who can join the NCT06001736 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Stroke, Ischemic. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06001736 currently recruiting?

Yes, NCT06001736 is actively recruiting participants. Contact the research team at Lauren.J.Sinks@hitchcock.org for enrollment information.

Where is the NCT06001736 trial being conducted?

This trial is being conducted at Lebanon, United States.

Who is sponsoring the NCT06001736 clinical trial?

NCT06001736 is sponsored by Dartmouth-Hitchcock Medical Center. The principal investigator is Jennifer Hong, Dr. at Dartmouth-Hitchcock Medical Center. The trial plans to enroll 95 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: April 2026  ·  Data Methodology