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Effect of Implementing Snap-needle Therapy Combined With Ginger Paste During Anesthesia Recovery on the Recovery of Gastrointestinal Function After Gynecologic Laparoscopy

Effect of Using Snap-Needle Therapy in Combination With Ginger Paste During Anesthesia Recovery on the Recovery of Gastrointestinal Function After Gynecologic Laparoscopy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06320613
Enrollment
150
Registered
2024-03-20
Start date
2024-03-20
Completion date
2024-09-20
Last updated
2024-03-20

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

Conditions

Gastrointestinal Motility, Postoperative Nausea and Vomiting

Keywords

Gastrointestinal Motility, Recovery of Function, PONV

Brief summary

The aim of this study was to investigate the effect of implementing snap-needle therapy combined with ginger paste during anesthesia recovery on the recovery of gastrointestinal function after gynecological laparoscopy.

Interventions

OTHERAcupuncture therapy

After disinfecting (alcohol or 0.9% Normal saline) the skin at the acupuncture point, use small tweezers to clip the handle of the needle, remove the adhesive tape and stab the acupuncture point at a perpendicular angle, and then press the thumb with moderate pressure on the snap-needle embedded needle site in order for the patient to feel localized soreness and distension as appropriate. The snap-needle was removed after 24 hours, and the pressing time point remained unchanged.

OTHERGinger Acupuncture Point Patch

Ginger was thinly sliced and then cut into 2-3cm diameter ginger discs according to a circular mold and covered with a sterile circular dressing. The ginger compress was removed within 6 hours.

Sponsors

Weifang People's Hospital
CollaboratorOTHER
Weifang Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. ASA I or II; 2. Performing gynecologic laparoscopic procedures under general anesthesia;

Exclusion criteria

1. Age ≤ 18 or ≥65; 2. The patient has a previous history of PONV, digestive disorders, etc; 3. Ulcers, infections, and skin tears at acupressure and acupuncture (snap-needle) treatment sites; 4. Patients allergic to ginger; 5. Inability to follow protocol or refusal to participant

Design outcomes

Primary

MeasureTime frameDescription
Postoperative nausea and vomitingMeasured at 0.5 hours postoperatively.The Index of Nausea and Vomiting and Retching (INVR) was used in this study. The scale consists of 8 items with 3 dimensions, which can quantify the number of occurrences, duration and severity of symptoms. The scale is scored using the Likert method, with a total of 32 points on a 5-point scale ranging from 0 to 4. The higher the score, the more severe the symptoms of nausea, vomiting, and dry heaving (entries 1, 6, and 7 are reverse scored). According to the score, nausea, vomiting and dry heaving symptoms can be categorized into five grades: 0, I, II, III and IV, and grade ≥I means that the symptom occurs. The severity and incidence of PONV at 0.5 hours postoperatively.
Abdominal distentionMeasured at 0.5 hours postoperatively.The severity and incidence of Abdominal distention at 0.5 hours postoperatively.
Time to first flatusApproximately 24 hours after surgery.Record the time of the first flatus. The earlier the time of first flatus, the earlier the time of recovery of gastrointestinal function.

Secondary

MeasureTime frameDescription
Postoperative pain responseMeasured at 0.5 hours postoperatively.The Visual Analog Score was used to assess pain response at 0.5 hours postoperatively. The score ranges from 0 (pain free or no pain) to 10 (worst pain).
Time to first defecationApproximately 24 hours after surgery.Record the time of first defecation.
Consumption of postoperative analgesicApproximately 24 hours after surgery.Record the type and dosage of postoperative analgesic within 24 hours after surgery.
Consumption of postoperative rescue antiemeticApproximately 24 hours after surgeryRecord the type and dosage of postoperative rescue antiemetic within 24 hours after surgery.

Countries

China

Contacts

Primary ContactLin Cheng, B.S
1318216353@qq.com17667404256

Outcome results

None listed

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