Effects of Ropivacaine Concentrations on Prolonged Labor Analgesia
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: High-concentration Ropivacaine, Low concentration ropivacaine group.
- Кому может быть актуально
- Состояния в реестре: Labor Analgesia, Prolonged, Ropivacaine, Concentration. Базовые параметры: от 18 лет · Женщины.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Китай
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Официальное название
Effects of Different Concentrations of Ropivacaine on Prolonged Labor Analgesia
Обзор
With the changes in medical models and improvements in people's quality of life, parturients have higher demands for childbirth, making the alleviation and elimination of labor pain an important aspect of modern obstetrics. Intrathecal labor analgesia has been widely adopted in clinical practice to relieve pain. However, current studies mainly focus on parturients who are just beginning to receive labor analgesia, while for those experiencing prolonged analgesia, medical institutions still use traditional formulations, lacking relevant guidelines or expert consensus. In such cases, prolonged waiting and anxiety may lower the pain tolerance of parturients, leading to an increased need for higher concentrations of local anesthetics. To address this clinical gap, this study aims to explore the effects of different concentrations of ropivacaine in prolonged labor analgesia and has designed a prospective randomized controlled trial (RCT) to provide evidence for improving the analgesic regimen for this group of parturients.
Подробное описание
Background:
With changes in medical models and improvements in quality of life, parturients have higher expectations for childbirth, making the alleviation and elimination of labor pain an important aspect of modern obstetrics. Intrathecal labor analgesia is widely used in clinical practice to relieve labor pain. However, studies on prolonged labor analgesia, especially following the replacement of the first analgesic pump, are scarce. Medical institutions often continue to use traditional analgesic formulations without relevant guidelines or expert consensus. Prolonged analgesia may reduce pain tolerance in parturients, possibly necessitating adjustments in local anesthetic concentration to improve analgesic effectiveness. Given the clinical research gap, this study aims to explore the effects of different concentrations of ropivacaine on prolonged labor analgesia and its impact on maternal and neonatal safety.
Objective:
To investigate the effects and maternal-neonatal safety of using different concentrations of ropivacaine for prolonged labor analgesia, providing clinical evidence for optimizing labor analgesia regimens.
Methods:
This single-center prospective randomized controlled study will collect clinical data from parturients receiving labor analgesia at Chengdu Jinjiang District Maternal and Child Health Hospital from May to August 2025. Participants meeting the inclusion and exclusion criteria will be included. Following the replacement of the first analgesic pump, parturients will be randomly assigned to receive one of two ropivacaine concentration regimens (Group H: 0.12% ropivacaine; Group N: 0.1% ropivacaine). Data collection will include demographic information, pain scores, labor-related parameters, neonatal outcomes, and adverse reactions.
Interventions:
1. Group H: 0.12% ropivacaine + 0.5µg/ml sufentanil 2. Group N: 0.1% ropivacaine + 0.5µg/ml sufentanil Following the replacement of the first analgesic pump, parturients will receive the respective ropivacaine concentration formulation, with pain relief effects and labor-related indicators assessed at specified intervals.
Primary Outcome:
Pain scores at different time points (T0: at pump replacement; T1: 0.5 hours after pump replacement; T2: 1 hour after pump replacement; T3: at full cervical dilation or during transition to cesarean section).
Secondary Outcomes:
1. Labor-related indicators: Duration of first, second, and third stages of labor, blood loss, rate of instrumental delivery, mode of delivery (vaginal/cesarean). 2. Neonatal indicators: Neonatal weight, Apgar scores at 1 minute, 5 minutes, and 10 minutes. 3. Adverse reactions: Hypotension, nausea/vomiting, intrapartum fever (T≥38.0℃).
Hypothesis:
Different concentrations of ropivacaine for prolonged intrathecal labor analgesia will have varying effects on pain control and maternal-neonatal safety, with higher concentration ropivacaine (0.12%) likely being more effective in pain relief, while both concentrations are expected to show no significant difference in maternal and neonatal safety.
Ethics Approval:
This study has received approval from the ethics committee of Chengdu Jinjiang District Maternal and Child Health Hospital (Approval Number: 202312). All participants must sign an informed consent form to ensure the respect of participant rights and data confidentiality. The study will strictly adhere to relevant ethical standards and legal regulations to protect participant safety and privacy.
Funding:
This study is funded by the following projects:
1. Chengdu Medical Research Project (No. 2023465) 2. Chengdu Medical Research Project (No. 2022548) 3. Chengdu Medical Research Project (No. 2023304)
Вмешательства
- Препарат High-concentration Ropivacaine
After the first pump fluid is depleted, switch to 0.12% ropivacaine to continue labor analgesia. - Препарат Low concentration ropivacaine group
After the first pump fluid is depleted, switch to 0.12% ropivacaine to continue labor analgesia.
Первичные конечные точки
- Visual Analog Scale (VAS) Pain Score [Срок оценки: From pump replacement to the end of labor analgesia.]
Вторичные конечные точки (4)
- Modified Bromage score [Срок оценки: From pump replacement to the end of labor analgesia.]
- Mode of delivery [Срок оценки: At the end of delivery]
- Neonatal Apgar score [Срок оценки: 10 minutes after the delivery of the fetus]
- nausea and vomiting questionnaire [Срок оценки: From pump replacement to the end of labor analgesia.]
Критерии участия
Критерии включения
- ASA II
- Age ≥ 18 years
- Singleton pregnancy
- No contraindications for epidural puncture and voluntarily accepting labor analgesia
- Maternal participants changing the first pump fluid
Критерии исключения
- Contraindications for epidural labor analgesia
- Serious heart, brain, liver, or kidney diseases
- Mental abnormalities
- Neurological diseases
- Maternal request for management of breakthrough pain before changing the pump fluid
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Четверное слепое
- Основная цель
- Лечение
Центры проведения
Китай · 1 центр
- Chengdu Jinjiang District Women & Children Health Hospital, — Чэнду
Публикации
- Jian Z, Longqing R, Dayuan W, Fei J, Bo L, Gang Z, Siying Z, Yan G. Prolonged duration of epidural labour analgesia decreases the success rate of epidural anaesthesia for caesarean section. Ann Med. 2022 Dec;54(1):1112-1117. doi: 10.1080/07853890.2022.2067353. PMID 35443838
- Ni JX, Feng JL, Yao SJ, Ni LF, Song SB, Song CZ, Qian XW, Mei Z, Yu J. Determination of the Dose-Response Relationship of Epidural Dexmedetomidine Combined with Ropivacaine for Labor Analgesia. Drug Des Devel Ther. 2022 Mar 6;16:609-618. doi: 10.2147/DDDT.S346842. eCollection 2022. PMID 35281318
- Tan HS, Reed SE, Mehdiratta JE, Diomede OI, Landreth R, Gatta LA, Weikel D, Habib AS. Quality of Labor Analgesia with Dural Puncture Epidural versus Standard Epidural Technique in Obese Parturients: A Double-blind Randomized Controlled Study. Anesthesiology. 2022 May 1;136(5):678-687. doi: 10.1097/ALN.0000000000004137. PMID 35157756
- Hawkins JL. Epidural analgesia for labor and delivery. N Engl J Med. 2010 Apr 22;362(16):1503-10. doi: 10.1056/NEJMct0909254. No abstract available. PMID 20410515
Идентификаторы
NCT: NCT07007650 · 202312