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The effect of oral consumption of honey water (ma-ol-asal) on postoperative complications and the quality of recovery in laparoscopic cholecystectomy

Phase 3
Recruiting
Conditions
aparascopic cholecystectomy.
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K80-K87
Registration Number
IRCT20211018052806N1
Lead Sponsor
Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
68
Inclusion Criteria

Laparoscopic gallbladder surgery,,,
age between 18 and 65 years
, NPO
BMI between 18 and 30,
PS patients one and two (either have no underlying disease or have controlled underlying disease)
tend to Participate in the study and give informed consent

Exclusion Criteria

Having vestibular symptoms (nausea caused by ear diseases)
Known gastrointestinal diseases (such as colitis, gastritis, etc.)
Drug and benzodiazepine addiction
Having nausea
Unawareness and having psychotic symptoms
Have a history of allergies to honey compounds (especially cinnamon or other plants with similar families)
Being pregnant while studying
Consumption of antiemetics and vomiting other than the treatment protocol
The patient's inability to continue cooperating for any reason, such as loss of consciousness, death of the patient
Inability of the patient to determine the severity of nausea and bloating despite the instructions
Complete lack of access to the patient
Changes in surgical procedures and intraoperative anesthesia for any reason

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea score based on visual analog scale. Timepoint: Upon entering the operating room, during recovery, 2 and 24 hours after surgery. Method of measurement: Visual analog scale.;Number of vomiting times based on patient observation. Timepoint: Upon entering the operating room, during recovery, 2 and 24 hours after surgery. Method of measurement: Patient observation.;Variable bloating score based on visual analog scale. Timepoint: Upon entering the operating room, during recovery, 2 and 24 hours after surgery. Method of measurement: visual analog scale.;Pain variable score based on visual analog scale. Timepoint: Upon entering the operating room, during recovery, 2 and 24 hours after surgery. Method of measurement: visual analog scale.;Recovery quality score based on QOR-40 questionnaire (40-200). Timepoint: 2, 12 and 24 hours after surgery. Method of measurement: Recovery Quality Questionnaire (QOR-40).
Secondary Outcome Measures
NameTimeMethod
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