Pain Clinical Trial
Official title:
Non-pharmacological Analgesia During Heel Prick: A Randomized, Controlled Trial
Verified date | April 2012 |
Source | Puerta de Hierro University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Spain: Ethics Committee |
Study type | Interventional |
Objective
To investigate the analgesic effect (measured with NIPS) of breastfeeding in addition to
skin-to-skin contact versus other methods of non-pharmacological analgesia during blood
sampling through heel lance in healthy term neonates. The influences of non-pharmacological
methods on crying time, percentage of crying while sampling, heart rate, number of attempts
and duration of sampling were studied.
Methods
Randomised controlled trial performed on 136 healthy term newborns in the maternity ward of
a tertiary hospital. The inclusion criteria were: healthy term neonates, wish to breastfeed
and absence of feeding during the previous 60 minutes. Neonates were randomly assigned to
four groups: group 1, breastfed with skin-to-skin contact ; group 2, oral sucrose with
skin-to-skin contact ; group 3, skin-to-skin contact ; or group 4, receiving oral sucrose
Data for the primary objective was analysed per intention to treat. This study was approved
by local ethical committee.
Status | Terminated |
Enrollment | 136 |
Est. completion date | April 2012 |
Est. primary completion date | February 2012 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 37 Weeks to 41 Weeks |
Eligibility |
Inclusion Criteria: - Healthy term neonates (37-41+6 weeks of gestation) confirmed through a routine physical exam during the first 24h of life - Wish to breastfeed - Absence of feeding during the previous 60 minutes. Exclusion Criteria: - Maternal use of opioids. - Birth in general anesthesia. - Artificial feeding. - Previous capillar or venous sampling. - Previous admission to the neonatal unit. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Spain | Hospital Universitario Puerta de Hierro-Majadahonda | Madrid |
Lead Sponsor | Collaborator |
---|---|
Puerta de Hierro University Hospital |
Spain,
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* Note: There are 30 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | NIPS score during heel prick in healthy term neonates | The NIPS scale is a validated 6-indicator scale for the assessment of acute pain in neonates. Score ranges from 0 (no pain) to 7 (severe pain). NIPS score was evaluated at three time points (2 minutes before heel prick (NIPS-t0), during heel prick (NIPS-t1) and 2 minutes after heel lance (NIPS-t2))in 4 groups where different methods of non-pharmacological analgesia were applied. Results are shown as mean+-SD. NIPS score =4 means moderate-severe pain. Thus results are also shown as the % of patients with NIPS score =4 at different time points (t0, t1 and t2) |
Midpoint analysis will be conducted when half the patients are recruited (134 subjects), at an estimated time of 12 months. | Yes |
Secondary | Crying time during heel prick in healthy term neonates | Crying time (in seconds) in 4 groups where different methods of non-pharmacological analgesia were applied. The timer was started at heel prick and stopped when 5 dried spots of blood were collected on a filter paper card. Results are shown as mean+-SD. | Midpoint analysis will be conducted when half the patients are recruited (134 subjects), at an estimated time of 12 months. | Yes |
Secondary | Percentage of crying during heel prick in healthy term neonates | Percentage of crying in 4 groups where different methods of non-pharmacological analgesia were applied during heel prick. Percentage of crying was defined as the ratio between crying time while sampling and time of the procedure. Results are shown as mean+-SD. | Midpoint analysis will be conducted when half the patients are recruited (134 subjects), at an estimated time of 12 months. | Yes |
Secondary | Heart rate during heel prick in healthy term neonates | Heart rate was monitored by a pulse oximeter (Radical MasimoSet Datascope, Masimo Corporation, Irvine, CA) set on the infant's hand or foot. Hear rate was measured continuously but special attention was given to three time points: t0 (2 minutes before sampling); t1 (the highest value of the first 10 seconds after heel prick); and t2 (2 minutes after the procedure). Results are shown as Mean+-SD | Midpoint analysis will be conducted when half the patients are recruited (134 subjects), at an estimated time of 12 months. | Yes |
Secondary | Sampling duration during heel prick in healthy term neonates | Sampling duration (in seconds) was defined as the time spent to obtained 5 dried spots of blood collected on a filter paper card. Results are shown as mean+-SD. | Midpoint analysis will be conducted when half the patients are recruited (134 subjects), at an estimated time of 12 months. | Yes |
Secondary | Number of attempts during heel prick | Number of attempts need to obtaine 5 dried spots of blood collected on a filter paper card. Results are shown as % of patients with 1 attempt and % of patients with 2 attempts. | Midpoint analysis will be conducted when half the patients are recruited (134 subjects), at an estimated time of 12 months. | Yes |
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