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NCT04930848

Effectiveness of Aqueous Extract(Tea) of Euphorbia Hirta (Dudhiya) in Improving Sleep Quality

Completed NA Last updated 24 June 2021
What this trial tests

NA trial testing Euphorbia hirta (Dudhiya) in Poor Sleep Quality in 32 participants. Completed in 10 May 2021.

Timeline
3 April 2021
Primary endpoint
27 April 2021
10 May 2021

Quick facts

Lead sponsorDr. Zannatun Nahar Nuri
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeother
Enrollment32
Start date3 April 2021
Primary completion27 April 2021
Estimated completion10 May 2021
Sites1 location across Bangladesh

Drugs / interventions tested

Conditions studied

Sponsor

Dr. Zannatun Nahar Nuri

Who can join

Adults 20 to 50, any sex, with Poor Sleep Quality. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Sound sleep is needed for our overall health and optimum our productivity. Sleep quality affects people's work performance, mood, safety, and quality of life. Changing times and advancements in technology couples with altered lifestyles have taken a toll on human health. Poor sleep quality reduces short-term memory, cognitive abilities, and motor skills for all age groups. The high prevalence of poor sleep quality in every age group has triggered a growing worldwide demand for a safe, effective and easily available herbal cure. Studies shown that, E. hirta has sedative action. For this, I hypothesized that oral intake of aqueous extract (tea) of E.hirta is efficacious in improving sleep quality. In this study I assessed the efficacy of aqueous extract (tea) of Euphorbia hirta (Dudhiya) in improving sleep quality in persons aged 20 to 50 years with self-reported sleep disturbance. The main objective of the study is to assess the efficacy of oral intake of aqueous extract of E.hirta in improving sleep quality in terms of having regular sound sleep and freshness in the daytime work. A total of 32 adults with poor sleep quality was recruited for this study and included both of male and female. Duration of the study was 05 months and active participation of each participant was 2 consecutive weeks or 14 days. Study area was included Dhaka, Narayanganj and Munshiganj districts and study center was Dr. Hakeem Md. Yousuf Harun Bhuiyan Hospital, Hamdard University Bangladesh.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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