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SNPMiner SNPMiner Trials (Home Page)


Report for Mutation M1106C

Developed by Shray Alag, 2020.
SNP Clinical Trial Gene

There is one clinical trial.

Clinical Trials


1 "Eye Protection After Mydriatic Use for ROP Screening: Impact on Vitals Signs and Pain Scores"

Pupillary dilation induced by mydriatic agents during Retinopathy of Prematurity exams can persist for hours. Despite regular use of eye protection for mydriatic-induced light sensitivity for infants, children and adults, eye protection after mydriasis has not been addressed in neonates. This study examines the use of eye patches to protect the dilated pupil from light exposure and their impact on vital signs and pain scores. prevents tachycardia, tachypnea and discomfort in neonates after ROP screening.

NCT01860534
Conditions
  1. Light Sensitivity
Interventions
  1. Behavioral: eye covers
MeSH:Photophobia
HPO:Photophobia

Heart rate was recorded directly from their cardio-respiratory monitor (Agilent M1106C). --- M1106C ---

Respiratory rate was recorded directly from their cardio-respiratory monitor (Agilent M1106C). --- M1106C ---

Oxygen percent saturation was recorded directly from their cardio-respiratory monitor (Agilent M1106C). --- M1106C ---

Primary Outcomes

Description: At 3 times (pre-mydriasis, 1 hour and 3 hours after Cyclomydril drops), subjects were exposed to ambient lighting for a period of five minutes. This usually entailed removing isolette covers and exposing the patient to the ambient room light. During this time, pain and vital signs were recorded every minute. Heart rate was recorded directly from their cardio-respiratory monitor (Agilent M1106C). The mean of the five recorded values for each variable was used

Measure: Heart Rate

Time: pre-mydriasis, 1 hour and 3 hours after mydriatic drops

Secondary Outcomes

Description: At 3 times (pre-mydriasis, 1 hour and 3 hours after Cyclomydril drops), subjects were exposed to ambient lighting for a period of five minutes. This usually entailed removing isolette covers and exposing the patient to the ambient room light. During this time, pain and vital signs were recorded every minute. Respiratory rate was recorded directly from their cardio-respiratory monitor (Agilent M1106C). The mean of the five recorded values for each variable was used

Measure: Respiratory Rate

Time: pre-mydriasis, 1 hour and 3 hours after mydriatic drops

Description: At 3 times (pre-mydriasis, 1 hour and 3 hours after Cyclomydril drops), subjects were exposed to ambient lighting for a period of five minutes. This usually entailed removing isolette covers and exposing the patient to the ambient room light. During this time, pain and vital signs were recorded every minute. Oxygen percent saturation was recorded directly from their cardio-respiratory monitor (Agilent M1106C). The mean of the five recorded values for each variable was used

Measure: Oxygen Percent Saturation

Time: pre-mydriasis, 1 hour and 3 hours after mydriatic drops

Description: At 3 times (pre-mydriasis, 1 hour and 3 hours after Cyclomydril drops), subjects were exposed to ambient lighting for a period of five minutes. This usually entailed removing isolette covers and exposing the patient to the ambient room light. During this time, pain and vital signs were recorded every minute. Pain scores were recorded by direct observation using the Neonatal and Infant Pain Scale (NIPS). The mean of the five recorded values for each variable was used. NIPS scoring consists of 6 measures associated with neonatal or infant pain, each with a range of 0-7 with low scores (0-2) associated with no pain and scores > to 4 associated with severe pain. Maximum scoring would be 42 for severe pain and minimal being 0 for no pain. The six measures on NIPS include: facial expression, crying, breathing patterns, arm movements, leg movements and state of arousal.

Measure: Pain

Time: pre-mydriasis, 1 hour and 3 hours after mydriatic drops


HPO Nodes


HP:0000613: Photophobia
Genes 323
NR2E3 RPGRIP1 ITM2B TGFBI KLRC4 TYR GUCY2D NR2E3 IL12A-AS1 ARL3 CNGA3 TUB RPGRIP1 CNNM4 RPGRIP1 CEP78 COL8A2 PRPF4 RP2 ERCC8 HLA-DRB1 ERCC6 DDB2 CACNA1F SLC39A4 NEK2 GJB2 PRPF3 PDE6B TOPORS MCOLN1 RDH12 CHST6 IFT172 ARL2BP TARS1 SLC1A3 PROM1 DKK1 GJB6 ZEB1 ARHGEF18 ABCA4 CTNS LRAT C8ORF37 CRX SEMA4A BBS2 CDHR1 AFG3L2 TP63 MCOLN1 XPA ERCC8 CNGB3 BEST1 HK1 RAX2 CNGA3 TTC8 CFAP410 FOXC2 GUCY2D SCAPER ZNF408 OCA2 GJB6 GUCA1A HARS1 GTF2E2 CA4 FOXC2 PITPNM3 AIPL1 RTN4IP1 NLRP3 OPN1MW CHST6 PDE6A GPR143 PRCD DHX38 RGS9 GPR143 LYST RHO CNGB3 TNF USH2A CLCC1 SLC7A14 OVOL2 KRT12 AP3D1 ERCC2 OPN1LW DRAM2 POC1B ERCC6 CACNA2D4 ATF6 GNAT2 PCARE CRX FAM161A DRAM2 RLBP1 ABCA4 VSX1 ATXN7 GNB3 KCNJ13 ERCC4 PLCD1 ERCC3 HPS6 POLH LRAT TIMM8A KIZ TP63 GUCY2D CDHR1 GUCA1A LYST ERCC3 RPE65 ZNF408 ERCC2 REEP6 GRHL2 MPLKIP RLBP1 PCNA IL10 PITPNM3 RPE65 RAX2 POMGNT1 OPN1SW CACNA1F SAG GJB6 TYR SEMA4A ANTXR1 AHSG CABP4 CST6 C8ORF37 HLA-B ESR1 TTLL5 RIMS2 AP1B1 CACNA2D4 ALMS1 KCNV2 CDHR1 XPA RPGR UNC119 GJB2 AIRE ROM1 LTBP2 PSAP IMPG2 ZNF513 IKZF1 CRYGC RP1 MEFV COL17A1 ERCC6 RPGR TYR AGBL5 TULP1 NMNAT1 ELOVL1 ERCC2 AHR CRX SPATA7 CRB1 KRT3 RGS9BP GALC ERCC5 CA4 MBTPS2 PRPH2 RP9 IMPDH1 MBTPS2 RAB28 GUCA1A POLH FAS MERTK PRPF31 KLHL7 PRPF6 SLC6A19 HADHA ERCC2 UBAC2 ADAM9 ITGB6 RPGR CNGA3 CEP250 PIKFYVE NOD2 STAT4 CFAP410 MBTPS2 CNGB3 GUCA1B HLA-B CTNS NRL TGFBI PDE6G NMNAT1 RBP3 ALMS1 EDNRA EYS ST14 CTNS KIAA1549 GNAT2 ALDH3A2 NLRP1 MAPT RPGR HGSNAT HLA-A CNNM4 TLR4 ERCC8 SLC24A5 MC1R CERKL PDE6C PCNA POLA1 RIMS1 RHO IDH3A RP1L1 ERAP1 TIMM8A SNRNP200 XPC LRMDA LSS CNGB1 CLRN1 OPN1LW EYS AP3B1 TTC8 C4A ERCC1 DDB2 PDE6H PNPLA6 IFT88 ARL6 AHI1 MAPT PRPF8 PRPH2 ATF6 SEMA4A MAK PCYT1A ATF6 SLC1A3 PRPH2 SCN1A SLC24A5 WNT10A PROM1 OPN1MW IL12A PRPH2 PRPH2 FOXE3 RNF113A PDE6C OFD1 TACSTD2 DHDDS ERCC6 SLC45A2 CCR1 MFRP ALDH3A2 RGR FSCN2 PDE6C PRPH2 TAT GNAT2 RDH5 OPN1LW IDH3B ERCC4 OPN1MW GTF2H5 PDE6H OVOL2 IL23R C8ORF37 IFT140 CNGA1 TYR XPC
Protein Mutations 1
M1106C
SNP 0