Skip to content

Comparison Between Aromatherapy Massage with Peppermint Oil and Sweet Almond Oil on Pain, Vomiting and Vital Signs after Laparoscopic Cholecystectomy Surgery

Comparisons between aromatherapy massage with peppermint oil and sweet almond oil on pain, nausea, vomiting and physiological parameters after Laparoscopic Cholecystectomy Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014021914802N2
Enrollment
60
Registered
2014-08-16
Start date
2013-12-22
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

Laparoscopic Cholecystectomy. Calculus of gallbladder without cholecystitis

Interventions

Intervention 1: For the intervention Group 1:After surgery as the patients experience postoperative pain and nausea, researcher washes and dries her hands and then applies petrissage by clockwise circ
Treatment - Other
For the intervention Group 1:After surgery as the patients experience postoperative pain and nausea, researcher washes and dries her hands and then applies petrissage by clockwise circular movements w
For Control Group 2: After surgery ,as the patients experience postoperative pain and nausea, the researcher washes and dries her hands and then applies petrissage by clockwise circular movements with

Sponsors

vice-chancellor for research and technology of Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : Being over 18 years of age; Ability to understand and speak Persian; No history of any previous gastrointestinal disorders; No history of motion sickness; Dizziness and lack of movement; Lack of drug addiction; No use of anticoagulant drugs; No hemorrhagic disease; History of eczema; History of dermatitis or psoriasis, scars and burns on the hands and feet; Failure to participate in the risk of aspiration and the incidence of illus(eg, background radiation, excessive sedation, Anastomosis and receiving) Exclusion criteria: Pain during the intervention; More patients withdrew from participation in the study; Need for blood transfusion in recovery room.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 0,6,12,24 hours after intervention. Method of measurement: Visual Analog scale.;Blood pressure. Timepoint: 0,6,12,24 hours after intervention. Method of measurement: Portable analog pressure gauge.;Nausea and Vomitting. Timepoint: 0,6,12,24 hours after intervention. Method of measurement: Visual Analog Scale.;Heart Rte. Timepoint: 0,6,12,24 hours after intervention. Method of measurement: Radial Pulse.;Respiratory rate. Timepoint: 0,6,12,24 hours after intervention. Method of measurement: Observation chest in a minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Adarvishi

Ahvaz Jundishapor University of Medical Sciences

sara.adarvishi@yahoo.com adarvishi.s@ajums.ac.ir+98 61 1377 7966

Outcome results

None listed

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