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A study to evaluate the role of zinc sulphate as analgesic in acute herpes zoster

Evaluation of analgesic effect of zinc sulphate in acute herpes zoster

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044798
Enrollment
48
Registered
2022-08-22
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B029- Zoster without complications

Interventions

Intervention1: zinc sulphate oral tablet: Study group: 24 patients with acute herpes zoster infection will receice zinc sulphate tablet 40mg od starting from the day of presentation along with the

Sponsors

Pt BD Sharma University of health and science PGIMS Rohtak Haryana
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: : Patients of age group > 18 years of either sex referred to Pain Clinic from Skin OPD after establishing the diagnosis of acute herpes zoster infection (fever, pain and maculo-papular/vesicular rash), presenting within first week of acute phase and willing to participate in the study will be included in this study.

Exclusion criteria

Exclusion criteria: 1.Patients with any other cause of fever 2.any history of severe medical illness (i.e. cardiac diseases, diabetes mellitus, liver disease, renal disease, CNS disorders) 3.Pregnant and lactating females 4. 4. Already taking any kind of zinc supplement, antiviral or analgesic other than standardized treatment

Design outcomes

Primary

MeasureTime frame
VAS score, pre and post administration of oral zinc sulphate tablet in patients with acute herpes zosterTimepoint: T0: at time of presentation T1: at end of first week of acute herpes zoster T2: at end of second week of acute herpes zoster T3:at end of third week of acute herpes zoster T4: at end of fourth week of acute herpes zoster

Secondary

MeasureTime frame
note and treat side effects of oral zinc sulphate, if any Timepoint: T0: at time of presentation T1: at end of first week of acute herpes zoster T2: at end of second week of acute herpes zoster T3:at end of third week of acute herpes zoster T4: at end of fourth week of acute herpes zoster

Countries

India

Contacts

Public ContactDr Cheshta Sangwan

Pt. BD Shrama PGIMS, Rohtak

cheshta.sangwan@gmail.com8743933449

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026