Postpartum Pain

3

Review clinical trials related to Postpartum Pain. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

THE EFFECT OF REIKI ON BREASTFEEDING, PAIN AND COMFORT AFTER CESAREAN SECTION

EFFECT OF REİKİ APPLİED DURİNG THE POSTPARTUM PERİOD ON BREASTFEEDİNG, PAİN, AND COMFORT IN WOMEN WHO DELİVERED BY CESAREAN SECTİON The aim of this randomized controlled trial is to determine the effect of Reiki applied to volunteer women after cesarean section on breastfeeding, pain, and comfort in the postpartum period. The main questions it aims to answer are: Is there a difference in postpartum breastfeeding, pain, and comfort between the group receiving Reiki and the group receiving standard care? Is there a difference in postpartum breastfeeding, pain, and comfort between the group receiving Reiki and the group receiving Sham Reiki? Participants will receive Reiki six times postpartum: three times one-on-one during their hospital stay, and remotely in the second, third, and fourth weeks. The control group will receive standard care. The Sham Reiki group will receive Reiki points applied by a person without Reiki knowledge.

Participants needed: 99
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Mar 3, 2026Locations: 1
Eligibility criteria

Mothers aged 18 and over, [+9]

Preeclampsia/eclampsia, active postpartum hemorrhage, sepsis/fever ≥38°C, [+7]

Status: Not yet recruiting

QR Code-Based Preoperative Education for Cesarean Birth: Anxiety, Pain, and Comfort

This study aims to evaluate the effect of QR code-based preoperative education on anxiety, postpartum pain, and comfort levels in women undergoing cesarean birth. Cesarean delivery is a common surgical procedure, and insufficient preoperative information may increase anxiety and negatively affect postoperative recovery and comfort. In this randomized controlled study, eligible pregnant women scheduled for elective cesarean birth will be assigned to either an intervention group or a control group. Women in the intervention group will receive preoperative education delivered through QR code-based digital materials, including information about the cesarean procedure, postoperative pain management, and comfort-enhancing strategies. The control group will receive routine care provided by the hospital. Anxiety levels will be assessed preoperatively, while postpartum pain and comfort levels will be evaluated after delivery using validated measurement tools. The findings of this study are expected to contribute to the development of accessible and effective educational interventions to improve maternal well-being and postoperative outcomes in cesarean birth.

Participants needed: 88
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Karabuk UniversityUpdated: Jan 26, 2026
Eligibility criteria

Pregnant women aged 18 years or older [+4]

Emergency cesarean birth or unplanned change to emergency surgery [+5]

Status: Recruiting

Post-cesarean Analgesia: Comparing Effectiveness of Staggered v. Simultaneous Therapies

Cesarean delivery is a commonly performed surgical procedure associated with worse postpartum pain when compared to vaginal birth. Uncontrolled postpartum pain is associated with increased neonatal and maternal risks. Multimodal non-opioid pain medications, including acetaminophen and non-steroidal anti-inflammatory drugs (NSAIDs) are the preferred first-line therapies. There is no standard practice, however, on best dosing schedules (ie staggered or different time v. simultaneous or same time). This protocol describes a randomized clinical trial aimed to determine whether staggered dosing of acetaminophen and NSAIDs in superior to simultaneous dosing in controlling post-cesarean pain.

Participants needed: 825
Trial details
Phase: Phase 4Age: 16+Biological sex: FemaleType: InterventionalSponsor: Thomas Jefferson UniversityUpdated: Sep 3, 2025Locations: 1
Eligibility criteria

>/= 34 weeks gestation [+2]

Contraindication to acetaminophen or NSAIDs [+6]