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A study to compare efficacy and tolerability of Oral Azithromycin versus Oral Doxycycline with topical Clindamycin in subjects with moderate to severe Acne Vulgaris

Not yet recruiting
Conditions
Disorder of the skin and subcutaneous tissue, unspecified,
Registration Number
CTRI/2018/05/013916
Lead Sponsor
Dr Apoorva
Brief Summary

Acne vulgaris is a chronic inflammatory disease of the pilosebaceous follicles, characterized by comedones, papules, pustules, nodules and often scars.Acne is commonly encountered in adolescents and young adults.Even though acne vulgaris donot cause any mortality but often there is significant physical and psychological morbidity like permanent scarring,poor self image,depression and anxiety as it commonly effects the face,back and chest.Therefore, early and effective treatment of acne lesions is vital to prevent facial scars that lead to cosmetic and psychological impact on the subjects.Inspite of the availability of various therapies,standard guidelines and recommendations, the outcome of these therapies are still unsatisfactory with regard to efficacy,tolerability,safety,adverse effects and bacterial resistance.There are a few  studies comparing efficacy and tolerability of pulsed oral azithromycin and doxycycline with topical clindamycin in Indian population and hence the present study is taken.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Willingness to give written informed consent and availability for regular followup.
  • Subjects with Acne Vulgaris of grade 2 and 3 as per the investigators global assessment scale.
  • Subjects must be willing to refrain from using all other topical Acne medications or antibiotics during the 8 week treatment period.
Exclusion Criteria
  • Subjects with severe acne, nodulocystic lesions, acne conglobate, acne fulminans, acne rosacea, secondary(drug induced) acne.ion ingestion.
  • Subjects with a history of hypersensitivity or allergy to any study medication ingredients.
  • Subjects who have participated in any investigational drug study within 30 days prior to baseline will be excluded from participation.
  • Female subjects who are pregnant,lactating or planning to become pregnant during study participation.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess and compare the efficacy and tolerability of oral Azithromycin and oral Doxycycline in subjects with grade 2 and 3 acne vulgaris8 weeks
Secondary Outcome Measures
NameTimeMethod
Quality of life will be assessed using DLQI score8 weeks

Trial Locations

Locations (1)

KIMS Hospital

🇮🇳

Bangalore, KARNATAKA, India

KIMS Hospital
🇮🇳Bangalore, KARNATAKA, India
Dr Apoorva
Principal investigator
9902333326
apoorvaprabhu89@gmail.com

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