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临床试验/NCT06371144
NCT06371144已完成2 期

A Randomized Control Trial on Intravenous Paracetamol Versus Intramuscular Tramadol as Intra Partum Labor Analgesia in Pregnant Women at Alex Ekwueme Federal University Teaching Hospital Abakaliki

Darlington-Peter Chibuzor Ugoji1 个研究点 分布在 1 个国家目标入组 194 人开始时间: 2022年6月3日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
194
试验地点
1
主要终点
Mean pain score

研究概览

简要总结

ABSTRACT BACKGROUND: Labor pain is one of the most excruciating pain experienced by women. It affects maternal psychology and the course of labor causing apprehension, anxiety, and stress. Therefore there is a need for a safe and effective analgesic with minimal maternal and fetal side effects like intravenous paracetamol which has been shown to have great analgesic effect in labour with minimal maternal and neonatal side effects.

OBJECTIVE: To compare intravenous paracetamol versus intramuscular tramadol as labour analgesia and to evaluate the incidence of side effects on mother and baby of both drugs.

METHOD: This would be a hospital based randomized controlled trial comparing intravenous paracetamol to intramuscular tramadol as labour analgesia in pregnant women in active phase of labour in the department of obstetrics and gynecology at Alex-Ekwueme Federal University Teaching Hospital and St. Patrick Mile 4 hospital, Abakaliki. A total of 194 pregnant women in active phase of labour will be included in study after fulfilling the inclusion criteria. These women will be divided into 2 groups of 97 each. Group A will receive a 100ml intravenous infusion containing 1000mg of paracetamol single dose over 15min. Group B: will receive intramuscular tramadol hydrochloride 100mg single dose. Pain intensity of women with both drugs will be noted before administration of drug, one hour, two hours and three hours after administration of drug using the visual analog scale. Perinatal outcome will also be recorded.

10 ANALYSIS AND RESULTS: Data will be collated, tabulated and then statistically analyzed using Statistical Package for Social Science (IBM SPSS) software (version 24, Chicago II, USA). Continuous variables will be presented as mean and standard deviation (Mean ± 2SD) or median and range as appropriate, while categorical variables will be presented as frequencies and percentages. Chi-square test( or Fisher's exact test where applicable) will be used for comparison between groups for categorical variables while student t test or Mann-Whitney U test will be used for comparison between groups for continuous variables KEYWORDS Labour analgesia, intravenous paracetamol, intramuscular tramadol, visual analog scale, neonate, side effects.

详细描述

METHODOLOGY STUDY DESIGN This will be open label randomized controlled study on the comparison of intravenous paracetamol versus intramuscular tramadol as labour analgesia at the Alex Ekwueme Federal University Teaching Hospital, Abakaliki and St Patrick's Mile 4 Hospital, Abakaliki where both the researcher and trial participants are fully aware of which treatment group the participants are in and what treatments are assigned to them. 3.2. STUDY BACKGROUND The study will be done at the Alex Ekwueme Federal University Teaching Hospital, Abakaliki (AE-FUTHA), Ebonyi state. Ebonyi state is one of the 5 south eastern states in Nigeria. It was created in 1996 and is inhabited predominantly by the Igbo tribe. Abakaliki is the state capital. The state has a population of about 3 million people and occupies a land mass of 5932 kilometers square. Majority of the inhabitants engage in subsistent farming, petty trading and civil service as their occupation. Literacy level generally is low while poverty is prevalent among this population. Alex Ekwueme Federal University Teaching Hospital, Abakaliki (AE-FUTHA) was established in December 2011 following the merger between the defunct Federal medical Centre, Abakaliki and then Ebonyi State University Teaching Hospital, Abakaliki. It receives referrals from all parts of the state and neighboring states of Abia, Benue, Cross-River and Enugu. There are 54 obstetric bed spaces including postnatal and antenatal wards. The hospital runs a busy obstetric unit which is composed of five teams that are subdivided into two units, each unit manned by at least three consultants, senior registrars, registrars and house officers. The department of Obstetrics and Gynecology runs antenatal clinics managed by consultants and resident doctors assisted by trained nurses, midwives and other health workers. The antenatal clinic holds from Monday through Friday with about 5000 antenatal registrations per year. Antenatal clients are booked and assigned to consultants according to the units/teams running antenatal clinic that day. Preliminary data showed that the hospital had 984 deliveries in 2021 with approximately 82 deliveries per month. St. Patrick's Mile 4 Hospital, Abakaliki was established in 1948. It is a missionary hospital managed by Reverend Sisters. It is one of the hospitals in which residents from the AE-FUTHA pass through for their labour ward posting and/or rural posting in obstetrics and gynecology. The obstetrics and gynecology department of the hospital is run by two obstetrician- gynecologists with senior registrars and registrars posted from AE-FUTHA as well as medical officers and the nursing staff. The hospital runs antenatal clinic on Mondays to Wednesdays. It had 2100 deliveries in 2021 with approximately 175 per month.

STUDY SITE The study will be conducted in the labour ward suites of AE-FUTHA and St. Patrick Mile 4 Hospital Abakaliki.

STUDY POPULATION Participants in this study will be drawn from the population of booked women admitted in active phase of labour at the Alex Ekwueme Federal University Teaching Hospital, Abakaliki and St Patrick Mile 4 Hospital, Abakaliki who meet the inclusion criteria. The patients will be selected once they come in active labour (cervical dilatation of greater or equal to 4cm). Parturients will be counseled at the antenatal clinic to present once they start having symptoms of labour. They are usually educated about labour analgesia during the antenatal clinic period and they will be further educated about this particular work by the chief researcher and research assistants. Once the parturient presents in labour and a diagnosis of active labour made, those who meet the inclusion criteria and consented will be recruited into the study. The details of the study they were educated about at the antenatal clinic will be further briefly explained to them before informed consent will be obtained. They will also be assured of confidentiality. A detailed history will be obtained and a thorough examination will be carried out on all the patients in labour. They will be assured of optimal care even if they did not consent to participate in the study

STUDY DURATION The study will last for a period of 3 months. This was extrapolated from the finding that AEFUTHA and St Patrick's Mile 4 Hospital had a total of 3084 labour deliveries in 2021. Approximately 257 labour deliveries per month for both hospitals.

INCLUSION CRITERIA

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

Double blinded

入排标准

年龄范围
15 Years 至 45 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Pregnant women carrying live singleton fetuses at 37-42 weeks' gestational age.
  • Pregnant women in active phase of labour; cervical dilatation ≥ 4cm
  • Spontaneous onset of labour.
  • Singleton pregnancy with vertex presentation

排除标准

  • Women with clinical evidence of cephalopelvic disproportion
  • Malpresentation
  • Multiple pregnancy
  • Previously scarred uterus (post myomectomy, post caesarean)
  • Preterm labour
  • Induced labour
  • Antepartum hemorrhage
  • Pregnancy induced hypertension
  • History of known allergy to tramadol and paracetamol or opioids
  • History of medical disorders
  • Fetal distress
  • Intrauterine fetal death
  • Refusal to give consent

研究组 & 干预措施

Paracetamol group

Experimental

Receive intravenous paracetamol intrapartum as labour analgesia

干预措施: Paracetamol (Drug)

Tramadol group

Active Comparator

Receive intramuscular tramadol intrapartum as labour analgesia

干预措施: Paracetamol (Drug)

结局指标

主要结局

Mean pain score

时间窗: 4hours following administration of each agent

A standardized scale will be used to asses the mean pain score

次要结局

未报告次要终点

研究者

发起方
Darlington-Peter Chibuzor Ugoji
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Darlington-Peter Chibuzor Ugoji

Dr

Alex Ekwueme Federal University Teaching Hospital

研究点 (1)

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