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Clinical Trial Summary

To compare the effect of subcutenous sterile water injection technique with the subcutaneous saline injection technique in the degree and duration of low back pain-relieving during childbirth


Clinical Trial Description

Study sample:

The convenience sample will be recruited randomly on the basic of odd number will have saline injection and even number will be given a placebo (Sterile water injection)

Setting:

Labor ward in Women's health center at Assiut university hospital

Study design:

Experimental Randomized control study

Sample size:

The sample size was calculated using the formula N= (Zα+Zβ)2 x 2p(1-p)÷d2 ,taking the level of significance as 5%, Zα=1.96 and power of the test as 80%, Zβ=0.84. p=0.113. A sample size of 165 in each group was calculated. Total of 330 women will be studied (165 in each arm) Inclusion criteria

- In labour (spontaneous or induced

- During first stageof labour

- Primary and multiparous women

- A term singleton pregnancy (between 37 + 0 and 41 weeks)

- Have a fetus in a cephalic presentation

- Experience back pain assessed by visual analogue scale VAS and Face pain analogue ( Warden V, Hurley AC, Volicer L.2003)

- Provide informed consent.

Exclusion criteria

- Multiple pregnancy

- Malpresentation (breech, transverse, shoulder)

- Previous CS

- Infection or inflammation at the injection sites or complications that could cause bleeding at injection site eg. Thrombocytopenia.

Study Tools:

1. Personal data questionnaire

2. Visual Analogue Scale and Face analogue scale

3. Satisfaction scale ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02813330
Study type Interventional
Source Woman's Health University Hospital, Egypt
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date February 2015
Completion date June 2016

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