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Effects of Pepper Gas Exposure in Non-combatant Bystanders.

Pepper Gas Exposure Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01922700
Enrollment
298
Registered
2013-08-14
Start date
2013-04-30
Completion date
2013-10-31
Last updated
2014-07-21

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

Conditions

Cough, Irritation in Skin, Irritation in Throat, Lacrimation

Keywords

Pepper spray, bronchospasm, lacrimation

Brief summary

Pepper sprays and pepper gas grenades are used by riot police at various places in the world for crowd control. Data about the acute effects based on human studies is extremely scarce. Kashmir valley in the northern Indian state of Jammu & Kashmir has witnessed political turmoil for the past 22 years and incidents of stone pelting are common wherein groups of youth indulge in stone pelting at the security personnel. While there have been previous episodes of fatalities associated with incidents of firing by the security personnel; non lethal methods are adopted routinely now. These include lathis, water cannons, tear gas and more recently the pepper gas grenades. The pepper grenades explode in the area and the adverse effects are perceived by the population in the area too who are even sitting in their homes. The study proposes to observe the health effects of the pepper gas exposure in non-combatant civilians.

Detailed description

Eligibility: History of exposure to a pepper grenade explosion. Exclusion: Participation in combat operation/ stone pelting/ demonstration.

Interventions

None listed

Sponsors

Sheri Kashmir Institute of Medical Sciences
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

All participants with a history of exposure to pepper gas grenade explosion

Exclusion criteria

Combatant role while exposure

Design outcomes

Primary

MeasureTime frame
Development of cough, irritation in throat, nasal irritation, nasal discharge, wheezing, breathlessness, hemoptysis, chest pain upon exposure or worsening of already existing cough, breathlessness, wheezing of a previous respiratory illness.24 hours

Secondary

MeasureTime frame
Duration of symptoms developed10 days

Other

MeasureTime frame
Development of other non-respiratory symptoms which include (but not limited to) skin irritation, skin rash, lacrimation, visual disturbances, vomiting, any other GI symptom, headache, fever, seizures or any other neurological symptom and their duration24 hours

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026