Clinical trial Recruiting at 1 site Phase 3 Interventional Ages 50 and up

Calcitonin added to standard care for acute herpes zoster

Official title: The Prophylactic Value of Subcutaneous Calcitonin in Acute Herpes Zoster Patients: A Randomized Controlled Trial

Run by Tanta University · NCT07655804 · Data updated 2026-11-12

Researchers test whether subcutaneous calcitonin, given with standard treatment, helps people 50 and older with acute herpes zoster see less pain and lower risk of long-term nerve pain.

Quick facts

PhasePhase 3
Study typeInterventional
Ages50 Years and up
SexAll
Enrollment168 (estimated)
SponsorTanta University
Academic / other
Locations1 site (Tanta, Gharbia Governorate)
StatusRecruiting
StartedJuly 1, 2026
Main results expectedApril 1, 2027
Study endsOctober 1, 2027
Registry record updatedJuly 6, 2026
Trial IDNCT07655804 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults 50 years or older with acute herpes zoster of less than seven days and moderate to severe pain, without coagulation, hepatic, cardiovascular, or renal contraindications to calcitonin.

Probably not a fit

Patients with contraindications to calcitonin or those unlikely to develop postherpetic neuralgia may derive little to no benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This phase 3 randomized trial investigates adding subcutaneous calcitonin to the usual care for adults with acute herpes zoster. Participants with rash for less than seven days and moderate to severe pain are assigned to receive calcitonin or saline in addition to standard treatment. The goal is to see if calcitonin reduces acute pain and lowers the chance of developing postherpetic neuralgia. The intervention is given in an outpatient setting, focusing on safer, non-epidural administration. The study leverages prior evidence of calcitonin’s analgesic effects in other conditions and explores its preventive potential for neuralgia after shingles.

Why it matters

Potential benefit: If successful, patients may experience better acute pain control and a reduced likelihood of postherpetic neuralgia.

How similar studies have gone: Prior reports suggest calcitonin can ease acute pain in other conditions, but no randomized trials have tested its preventive role for postherpetic neuralgia in shingles.

Who can join: the full rules

Show full inclusion / exclusion 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.

Where it's running

  • Tanta University Hospitals
    Tanta, Gharbia Governorate, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.