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Effect of Recolic syrup on anxiety, sleep quality and vital signs after surgery in patients with limbs fracture

Effect of Recolic syrup on anxiety, sleep quality and vital signs after surgery in patients with limbs fracture

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190426043375N2
Enrollment
100
Registered
2020-03-26
Start date
2020-04-08
Completion date
Unknown
Last updated
2020-04-21

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: pain. Condition 3: Sleep. Condition 4: Fractures of the limbs. Anxiety disorder due to known physiological condition Acute pain, not elsewhere classified Sleep disorders not due to a substance or known physiological condition Fractures involving multiple regions of upper limb(s) with lower limb(s)

Interventions

Intervention 1: Intervention group: After awakening patients after surgery and observing fasting time as instructed by related doctor and checking reflex of gag returning, at first the patients will b

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 18 years and over Simple fracture in an area of the arm that has undergone internal fixation surgery to repair this fracture No Chronic Pain mental health No vision problems Absence of motor diseases No allergy to chamomile and anisum

Exclusion criteria

Exclusion criteria: Drug addiction disinterest or withdrawal during the study

Design outcomes

Primary

MeasureTime frame
Level of anxiety. Timepoint: Before the intervention, 6 hours after the intervention, 12 hours after the intervention. Method of measurement: Spielberger Anxiety questionnaire.;Vital signs. Timepoint: Before the intervention, 6 hours after the intervention, 12 hours after the intervention. Method of measurement: It is clinically evaluated.;Postoperative pain. Timepoint: Before the intervention, 6 hours after the intervention, 12 hours after the intervention. Method of measurement: Visual Analog Scale for Pain.;Sleep quality. Timepoint: The morning after surgery. Method of measurement: St. Mary's Hospital Sleep Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNima Abbasi veldani

Arak University of Medical Sciences

Nima.abbasi69@gmail.com+98 86 3417 3507

Outcome results

None listed

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