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The Impact of Preoperative Aromatherapy Upon Time to First Analgesia Request After Cesarean Section

The Impact of Preoperative Aromatherapy Upon Time to First Analgesia Request and Consumption After Cesarean Section; Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06114472
Enrollment
60
Registered
2023-11-02
Start date
2023-10-31
Completion date
2024-05-30
Last updated
2023-11-07

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

Conditions

Pain

Brief summary

one of the main aims of anesthesia is to reduce postoperative pain. However, many drugs that are used for this purpose, especially opioids, have side effects such as respiratory distress, nausea, itching, and gastrointestinal bleeding . Recent studies have indicated interest in using complementary therapies such as heat and cold therapy, hypnotism.

Detailed description

Pain is amongst the most common problems after surgery (1). Pain is an unpleasant sensory and emotional experience, which is associated with the real or probably damage of tissue. Unrelieved postoperative pain in addition to creating fears in the surgical patients, it makes adverse psychological impact on them * The uncontrolled postoperative pain will make a lot of acute and chronic effects, including systemic mediators, hypercoagulability, postoperative immunosuppression, and delayed wound healing * So, one of the main aims of anesthesia is to reduce postoperative pain. However, many drugs that are used for this purpose, especially opioids, have side effects such as respiratory distress, nausea, itching, and gastrointestinal bleeding. Recent studies have indicated interest in using complementary therapies such as heat and cold therapy, hypnotism.

Interventions

DRUGaromatherapy blend containing Lavender

hree drops of aromatherapy blend containing Lavender essence 10% were poured on cotton in cast containers, and the patient was asked to inhale it for 5 minutes from a distance of 10 cm

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Age between 20 and 40 years * Body mass index (BMI) of 18-35 kg/m2 * Patients with the American Society of Anesthesiologists (ASA) physical status I/II, * Patients scheduled for elective cesarean section.

Exclusion criteria

* Patient refusal * Allergy to local anaesthetics * Anosmia * Coagulopathy, * Chronic pain syndromes * Prolonged opioid medication * Patients who received any analgesic 24 h before surgery.

Design outcomes

Primary

MeasureTime frameDescription
time to first analgesia request24 hourstime to first analgesia request in minutes

Secondary

MeasureTime frameDescription
Total daily consumption of analgesia24 hoursintravenous keteloac total consumption in the 1st 24 hours

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026