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Assessment of likelihood ratio for four characteristic Carcinosin symptoms in Insomnia cases.

Assessment of Likelihood Ratio for Four Characteristic Carcinosin Symptoms in Insomnia Cases - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097304
Enrollment
100
Registered
2025-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: F510- Insomnia not due to a substance orknown physiological condition

Interventions

Intervention1: CARCINOSIN in insomnia cases: Doses: As required for patient Frequency: As per need of patient Route of administration: Oral Duration: 6 months Control Intervention1: Not applicable:

Sponsors

National Institute of Homoeopathy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participant suffering from insomnia verified by DSM5 criteria Severity Clinical Insomnia Severity Index (ISI) score more than or equal to 14 (moderate to severe insomnia) participants aged 18 to 60 years, all sexes. Subjects of all socioeconomic status, all religions Ability to understand either Bengali, Hindi, and or English participants giving written consent to participate in this study Subjects who agree to undergo laboratory investigation whenever required

Exclusion criteria

Exclusion criteria: Participants with unstable psychiatric disorder like severe intellectual disability or autism with severe behavioral disturbances, substance-induced severe psychiatric disorders. Pregnant women and lactating women. Immune compromised state like HIV AIDS (low CD4 count), Cancer (hematologic or solid tumors) on active treatment, Chronic kidney failure (end-stage renal disease) Concurrent medications: Use of hypnotics, sedatives, or stimulants that may interfere with sleep assessment. Participants who has taken homoeopathic medicines for any chronic illness within 3 months.

Design outcomes

Primary

MeasureTime frame
To assess the prevalence of selected symptoms of carcinosin in population that suffering from insomnia and improved by carcinosin ,assessment done through ISI [insomnia severity index].Timepoint: At baseline 3 months and 6 months

Secondary

MeasureTime frame
To evaluate the effectiveness of homoeopathic medicines in insomnia To evaluate the effectiveness of carcinosin or other indicative medicine on quality of life through ORIDL [Outcome Related to Impact on Daily Living].Timepoint: At baseline 3 months and 6 months

Countries

India

Contacts

Public ContactDr PRATIMA PAL

National Institute of Homoeopathy

dr.pratimapal@gmail.com7679507608

Outcome results

None listed

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