Current partner codePEPTIDESDE
NCT07655804·Phase 3·INTERVENTIONAL

Subcutaneous Calcitonin in Acute Herpes Zoster

Status

Recruiting

Phase

Phase 3

Enrollment

168

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

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.

Full detailed description

Herpes zoster is associated with inflammation of the dorsal root ganglion and peripheral nerves, and this inflammation is considered to be an important causative factor for postherpetic neuralgia. Interventions aimed at reducing this inflammation should therefore be effective in decreasing the likelihood of developing postherpetic neuralgia. Epidural administration of corticosteroids and local anesthetics has been shown to be effective, but is associated with the risk of arachnoiditis. Subcutaneous injection in an outpatient setting may be effective in preventing postherpetic neuralgia and is also considerably safer. Calcitonin has previously been shown to be effective in the management of acute pain following amputation. Also it was used in a previous study to prevent complex regional pain syndrome in severe hemiplegic patients after stroke. Also, a previous case report revealed that IV calcitonin provided immediate and sustained improvement in post herpetic neuralgia for over two months, without adverse effects from the calcitonin therapy. However, no previous trials evaluated the effect of subcutaneous calcitonin as a preventive measure against the development of postherpetic neuralgia. We will conduct this study as we hypothesize that calcitonin therapy in patients with acute herpes zoster may be associated with better acute pain control and therefore may decrease the incidence of postherpetic neuralgia.

Interventions

Treatment arms and agents.

DRUG

Calcitonin

patients will receive subcutaneous salmon calcitonin 100 IU (ampoule = 1 ml) daily for three weeks

OTHER

Saline

patients will receive subcutaneous saline (1 ml) daily for three weeks.

Timeline

From registration to results.

  1. First posted

    Jun 18, 2026

  2. Study start

    Jul 1, 2026

  3. Primary completion

    Apr 1, 2027

  4. Study completion

    Oct 1, 2027

  5. Results posted

    Not reported

  6. Registry updated

    Jul 6, 2026

Outcomes

What the study measures.

Primary outcomes

Incidence of postherpetic neuralgia at 3 months after rash onset.

Time frame · 3 months after onset of acute herpes zoster rash.

A numeric rating scale (NRS) that ranged from 0 for "no pain" to 10 for "worst ever pain will be used to assess the degree of pain. Pain score more than (3) at 3 months after onset of acute herpes zoster rash will be considered positive for the occurrence of postherpetic neuralgia.

Secondary outcomes

Incidence of postherpetic neuralgia.

Time frame · 6 months after onset of acute herpes zoster rash.

Pain score more than 3.

Severity of acute herpes zoster pain.

Time frame · Up to 1 month after onset of acute herpes zoster rash.

A numeric rating scale (NRS) that ranged from 0 for "no pain" to 10 for "worst ever pain will be used to assess the degree of pain.

Number of medications used to treat pain.

Time frame · up to 6 months after onset of acute herpes zoster rash.

Analgesics, anti-neuropathic pain medications and opioids will be recorded.

Side effects

Time frame · Up to 1 month after onset of acute herpes zoster rash.

Vomiting

Eligibility

Who can take part.

Minimum age
50 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

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.

Study locations

1 registered sites.

Egypt. Showing up to 24 locations stored in the fast local snapshot.

Tanta University Hospitals

Tanta, Gharbia Governorate, Egypt

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Calcitonin.

Related PeptideStat pages

Put the record in context.

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