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Labor Pain clinical trials

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NCT ID: NCT04728048 Recruiting - Anesthesia Clinical Trials

Dural Puncture Epidural VS Standard Epidural on Physician Top-ups During Labour Analgesia

DPE
Start date: January 19, 2021
Phase: N/A
Study type: Interventional

The purpose of this prospective randomized controlled study is to compare the number of physician top-up interventions during the first stage of labour between two different neuraxial analgesia techniques : the dural puncture epidural and the standard epidural.

NCT ID: NCT04716660 Completed - Labor Pain Clinical Trials

Changes in Sensory Block Level During a Programmed Intermittent Epidural Bolus Regimen for Labor Analgesia: an Observational Cohort Study

Start date: February 2, 2021
Phase:
Study type: Observational

Epidural analgesia is widely used for managing pain during labor. The programmed intermittent epidural bolus (PIEB) technique has been shown to produce less consumption of local anesthetics, better sensory block, less motor block, and increased maternal satisfaction than other epidural analgesia techniques. Despite all benefits from PIEB, such practice has been associated with high sensory block levels. Therefore, assessment of the sensory block level is an essential component of clinical safety. The lack of a standardized technique and timing to assess the sensory block level can lead to inappropriate management. The purpose of this study is to investigate the changes in block level over time, during cycles of a PIEB regimen. The investigators hypothesize that these levels will be highest soon after the PIEB bolus and lowest preceding the subsequent PIEB bolus. The investigators also want to investigate a possible correlation between these changes in sensory block levels and motor block, pain scores, and rescue bolus of local anesthetics.

NCT ID: NCT04662450 Withdrawn - Labor Pain Clinical Trials

Evaluation and Management of Parturients' Pain Intensity

Start date: September 2024
Phase: N/A
Study type: Interventional

The primary objective of this study is to examine the effects of Attentional Bias Modification (ABM) on the labor pain in parturients. One-third of the participants will undergo ABM training away from affective pain stimuli. One-third of the participants will undergo ABM training away from sensory pain stimuli. The rest of participants will be the control group.

NCT ID: NCT04662424 Recruiting - Labor Pain Clinical Trials

Effect of Music in Labor in Women Who Underwent Induction of Labor

Start date: December 3, 2020
Phase: N/A
Study type: Interventional

Women's experience of pain during labor varies greatly, and pain control is a major concern for obstetricians. Several methods have been studied for pain management for women in labor, including drug and non-drug interventions Most methods of non-pharmacological pain management are non-invasive and appear to be safe for mother and baby, including immersion in water, relaxation, acupuncture, and massage. However, their efficacy is unclear, and based mostly on non-randomized studies. On the other hand, there are strong data to support the efficacy of pharmacological methods, including epidural analgesia, which improves pain relief but increase the incidence of operative vaginal delivery Recently a clinical trial showed that music in labor was associated with maternal benefits in women who underwent spontaneous vaginal delivery. However, the effect of music in labor in women undergoing induction of labor is still a subject of debate.

NCT ID: NCT04645823 Completed - Labor Pain Clinical Trials

Spinal Fentanyl or Epidural Analgesia in the Early First Phase of Induced Labor

Start date: March 26, 2021
Phase: Phase 4
Study type: Interventional

A total of 60 parturients undergoing induction of labour will be consented to participate in the study where they will be randomized to receive either spinal fentanyl (20 µg) or epidural analgesia (fentanyl 100µg and lidocaine 80 mg). They will be monitored for the development of analgesia for a duration of 30 minutes.

NCT ID: NCT04637386 Completed - Obstetric Pain Clinical Trials

TAP Block vs LAWI for Analgesia Post-cesarean Section: RCT

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Adequate pain control after cesarean delivery is a significant concern both for parturients and obstetric anesthesiologists. Transversus Abdominis Plane (TAP) block and local Wound infiltration with anesthetics are alternatives for reducing the severity of pain, total analgesic consumption, and opioid side effects. Both the TAP block and wound infiltration are superior to placebo; however, it is unknown which provides better analgesia after cesarean delivery because of a scarcity of randomized clinical trials. So, we hypothesized that the TAP block would decrease postoperative pain and postoperative cumulative opioid consumption at 24 hours

NCT ID: NCT04611451 Completed - Pain Clinical Trials

Effect of Whole Body Vibration Exercises for Patients wıth Chronic Nonspeific Low Back Pain

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Whole body vibration (WBV), which is a new treatment method and applied through the device, is defined as mechanical repetitive motion or oscillatory motion occurring around a balance point (5). Chronic nonspecific low back pain is still a serious clinical, social and economic health problem. There are few studies and limited evidence evaluating the effectiveness of WBV exercises in chronic nonspecific low back pain. Different protocols are used for wbv exercise in studies (6). Our aim is to compare the effects of whole body vibration exercise modality on pain, functional recovery, laboor impact, quality of life with control group in patients with chronic nonspecific low back pain.

NCT ID: NCT04608006 Completed - Analgesia Clinical Trials

Epidural Analgesia and Delivery of Second Twin

Epidural
Start date: November 3, 2014
Phase:
Study type: Observational [Patient Registry]

Over an 8-year period, 124 twin pregnancies at gestational age ≥32 weeks with both twins presenting as a vertex and eligible for vaginal delivery were reviewed. Excluded were patients with the following intrapartum factors which may affect mode of delivery of second twin: 1. Presentation of the 2nd twin: breech or other than vertex; 2. Monochorionic twins; 3. Induction of labour; 4. difference in foetal weight between twin B and twin A ≥25%. The chi-square statistic was used to compare differences in the incidence of retained second twin between the groups.

NCT ID: NCT04556643 Completed - Labor Pain Clinical Trials

Effectiveness of Breathing Exercises During the Second Stage of Labor

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

To determine effectiveness of breathing exercises for pregnant women during the second stage of labor on maternal pain, duration of labor, dyspnea, oxygen saturation (SPO2) and the first-minute Appearance, Pulse, Grimace, Activity and Respiration (APGAR) scores

NCT ID: NCT04543487 Completed - Vaginal Delivery Clinical Trials

Therapeutic Touch on Labour Pain, Anxiety and Childbirth Attitude

touch
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Introduction: Touching ensures physical, emotional and spiritual relaxation, confidence, peace, calmness and well-being, and increases self-esteem. The aim of this study is to determine the effect of therapeutic touch on labour pain, anxiety and childbirth attitude. Methods: The sample of this randomized controlled experimental research consisted of 80 (intervention group: 40; control group: 40) women. Data were collected using a Personal Information Form, Visual Analogue Scale, State Anxiety Inventory and Childbirth Attitudes Questionnaire.