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The effect of Rosa damascene extract on anxiety rate and sleep quality, candidate angiography

The effect of Rosa damascene extract on anxiety rate and sleep quality candidate angiography:A double-blind randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015112425221N1
Enrollment
90
Registered
2016-02-02
Start date
2015-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: anxiety. Condition 2: sleep quality. anxiety NOS Nonorganic sleep disorders

Interventions

Intervention 1: In intervention group, Damascene Rose extract in oral drop, Construction Barij Essence Pharmaceutical Company(every 8 hours,15 drop with a little of water will be given. Intervention 2
Treatment - Drugs
Placebo
In intervention group, Damascene Rose extract in oral drop, Construction Barij Essence Pharmaceutical Company(every 8 hours,15 drop with a little of water will be given.
In control group, placebo in oral drop form, every 8 hours, 15drop with a little of water will be given. Placebo is similar to extract and it is made by Barij Essence Pharmaceutical Company.

Sponsors

Ardabil medical university,Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion / Exclusion: Inclusion criteria: age above 18 years with cardiac disease, candidate angiography, absence of angiography history and in their family, literacy, signing the informed consent sheet, absence of anxiety and sleep disorders, alert patients, at least 24, hours hospitalization .Exclusion criteria: Asthma and allergy history, using complementary medicine in recent week, using sedative and hypnotic medicine, critical ill and cancellation of work.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before and after intervention,before angiogeraphy. Method of measurement: Eshpilberger questioner.;Sleep quality. Timepoint: The night before and after intervention. Method of measurement: sent merrys hospital sleep questioner.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsoodabeh Babaee

School of nursing and midwifery Ardabil

babaei.s.110@gmail.com Tazakori@arums.ac.ir+98 45 3372 6085

Outcome results

None listed

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