Clinical Trials Directory

Trials / Completed

CompletedNCT07125742

Effects of Chewing Gum, Fennel, and Ginger Tea on Intestinal Motility and Comfort After Cesarean

The Effect of Chewing Gum, Fennel Tea, and Ginger Tea Consumption on Intestinal Motility and Postpartum Comfort in Women After Cesarean Section: A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
128 (actual)
Sponsor
Uşak University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This randomized controlled trial aims to evaluate the effects of chewing gum, fennel tea, and ginger tea consumption on intestinal motility and postpartum comfort in women following cesarean section. The primary research questions to be answered are: Do chewing gum, fennel tea, or ginger tea accelerate the onset of bowel sounds after cesarean section? Do these interventions affect the time to first gas passage, defecation, and feeling of hunger? Are there differences among these interventions in terms of their impact on abdominal distension and postpartum comfort? Researchers will compare the effects of the interventions between three groups: chewing gum, fennel tea, and ginger tea. Participants: Women who underwent cesarean section and voluntarily agreed to participate in the study. A total of 96 participants were randomly assigned into three groups of 32 each. Interventions and procedures: Starting 6 hours after cesarean section (following first oral fluid intake), at the 8th and 10th hours: The chewing gum group was asked to chew sugar-free gum for 15 minutes at each time point. The fennel tea group received 2 g of fennel steeped in 150 ml boiling water for 10 minutes. The ginger tea group received 2 g of fresh ginger steeped in 150 ml boiling water for 10 minutes. Bowel sounds were auscultated before and 60 minutes after each intervention. The time of first gas passage, first defecation, and first feeling of hunger was recorded. Abdominal distension was assessed using a Visual Analog Scale (VAS) six times in total (before and 60 minutes after each intervention). Postpartum Comfort Scale was applied to all participants at the 12th hour post-cesarean. All data were collected by the researchers. Randomization was supported by a healthcare professional not involved in the study.

Detailed description

This study was conducted to evaluate the effects of chewing gum, fennel tea, and ginger tea consumption on intestinal motility and postpartum comfort in women following cesarean section. Between November 2024 and August 2025, a randomized controlled trial was carried out with 128 women who met the inclusion criteria and had undergone cesarean delivery. Participants were randomly assigned to four groups (chewing gum, fennel tea, ginger tea, and control; n = 32 per group). Interventions were administered at the 6th, 8th, and 10th hours post-cesarean. The chewing gum group was instructed to chew sugar-free gum for 15 minutes at each time point. In the herbal tea groups, 2 grams of either fennel or fresh ginger were steeped in 150 ml of boiling water for 10 minutes and consumed accordingly. Bowel sounds were assessed before and 60 minutes after each intervention. Time to first flatus, first defecation, and first feeling of hunger were recorded. Abdominal distension severity was evaluated using a Visual Analog Scale (VAS) a total of six times-before and after each intervention. At the 12th hour postpartum, the Postpartum Comfort Scale was administered to all participants. Data were collected by the researchers, and randomization was supported by a healthcare professional not involved in the study.

Conditions

Interventions

TypeNameDescription
OTHERChewing gumThe chewing gum group was asked to chew sugar-free gum for 15 minutes at each time point.
OTHERFennel TeaFennel Tea: The fennel tea group received 2 g of fennel steeped in 150 ml boiling water for 10 minutes.
OTHERGinger TeaGinger Tea: The ginger tea group received 2 g of fresh ginger steeped in 150 ml boiling water for 10 minutes.

Timeline

Start date
2024-11-18
Primary completion
2025-08-16
Completion
2025-08-16
First posted
2025-08-15
Last updated
2025-09-08

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07125742. Inclusion in this directory is not an endorsement.