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Not Yet Recruiting NCT07655804

Subcutaneous Calcitonin in Acute Herpes Zoster

Conditions: Calcitonin, Subcutaneous, Acute Herpes Zoster

Sex: All
Ages: 50 Years – N/A
Healthy volunteers: No
Phase: PHASE3
Enrollment: 168
Sponsor: Tanta University

Location: Tanta University Hospitals Tanta Gharbia Governorate

Summary

This prospective randomized controlled study will be conducted to evaluate the effect of adding calcitonin to the standard treatment protocol in patients with acute herpes zoster infection.

Eligibility Criteria

Inclusion Criteria: * patients aged ≥ 50 years, with acute herpes zoster infection (rash duration \< 7 days) and moderate to severe pain. Exclusion Criteria: * Coagulation abnormalities * Pre-existing other pain syndrome or psychological disorders. * Severe hepatic, cardiovascular, or renal disorders. * Allergy to calcitonin.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07655804). StuddyBuddy aggregates publicly available trial information.